Participants
Objective 1:
Parents, Co-Parents, and Children. Families including parents, their children under the age of 36 months, and their identified co-parenting support persons are our study population.
Objective 2:
Knowledge Users. These include parents, health care professionals, and administrators from community partner agencies who participate in receiving or delivering the ATTACH™ Online program.
Stakeholder Engagement:
Building on our pilot work, we systematically engage stakeholders in our study planning design. Stakeholders and researchers engaged in multiple meetings at formative stages. Together, we identified ATTACH™ Online agencies for training and delivery, made changes to the ATTACH™ Online program, designed terms of reference, and selected the outcomes of interest. Key stakeholders include the Principal Knowledge User (Reimer) and members of the Community Engagement Committee. Reimer is Executive Director of the Alberta Council of Women’s Shelters, the provincial network organization of women's domestic violence shelters in Alberta that serves 40 members operating 50 agencies. She connected the team with 7 participating shelters whose leaders (e.g., administrators such as Executive Directors and health and social service professionals) are key community knowledge users on the Community Engagement Committee. Other Community Engagement Committee members are agency leaders operating services for teen mothers or families affected by significant adversity and trauma, as well as parents with relevant personal experience. These team members will participate in project roll-out, may participate in interviews as participants, learn about implementation, and/or have opportunities to take part in ATTACHTM Online training and ultimately independent delivery and evaluation. GRIPP-2SF (Preston et al., 2023; Staniszewska et al., 2017) will be used to report on study engagement.
Study Setting {9}
Settings include approximately eight Alberta agencies serving culturally diverse clients (i.e., Caucasian, Black, Indigenous, People of Colour [BIPOC], and immigrants) affected by family violence, depression, and low-income.
Eligibility Criteria {10}
Objective #1: The study inclusion criteria are: (1) parents with children between birth to 32 months of age at enrollment (our age ceiling is 36 months, based on selection of age-appropriate tools for assessing children); (2) parents who agree to participate in the ATTACH™ Online program consisting of 10 weeks of one-hour per week parent training sessions; (3) parents who agree to bring a co-parent for 2 of the 10 sessions; and (4) parents who are proficient in speaking and reading English.
Objective #2: Participants (i.e., parents, co-parents, community health and social service agency administrators, and health and social service providers) must be adults (18 years of age or older), proficient in speaking and reading English, and knowledgeable or experienced in parenting programs.
Intervention {11a, 11b, 11c and 11d}
To deliver the ATTACH™ Online program, health and social service professionals (knowledge users) in collaborating agencies are required to undergo 40 hours of online and in-person training with ATTACH™ Master Trainers (e.g., Hart), over 2-3 months. After completion of all requirements, these knowledge users are certified Facilitators, able to deliver the ATTACH™ Online program and collect evaluation data. They will deliver the intervention independently but supported by ATTACH™ Master Trainers. ATTACH™ Online sessions with parents take one hour, occur weekly over 10 weeks and include three components including discussions of: (1) Digital video recordings of 3–5-minute parent-child play sessions, (2) Hypothetical, mildly stressful situations (e.g., infant feeding challenges), and (3) Day-to-day real-life stressful situations of parents’ choosing (for details, see published papers: Anis et al., 2021; Anis, Letourneau, et al., 2020; Anis, Ross, et al., 2022; Letourneau et al., 2023; Letourneau, 2020). During sessions, certified ATTACH™ Facilitators explore the parents’ perceptions of themselves and their children’s thoughts, feelings, intentions, and mental states, to maximize opportunities to practice RF. For example, a mother may be asked to consider what may be happening in her mind and the mind of her child during a shared smile in the video recorded interaction. After establishment of a therapeutic relationship with the ATTACHTM Facilitators (typically after 6 sessions), parents invite their co-parenting support person to attend 2 sessions, usually sessions 7 and 9. Social support (e.g. information about community resources, emotional and affirmational support) is also provided as needed. Our goal is to have at least 2 health care professionals at each of the eight agencies trained to deliver the ATTACH™ Online program (for a total of 20 ATTACHTM Facilitators trained in online delivery).
Outcomes {12 including 12.1, 12.2, 12.3, 12.4, and 12.5}
A robust data collection protocol was developed during the ATTACH™ Online pilot, revealing that measures are feasible to effectively administer online and with REDCap (www.project-redcap.org).
Objective 1 Primary Outcome
Children’s Development. We will employ the parent-report ASQ-3 (Bricker & Squires, 2009) to assess newborn to 36-month-old children’s development. The ASQ-3 measures cognitive (i.e. communication, personal-social skills, problem solving) and motor (i.e. gross and fine) domains of development. The ASQ-3 is suitable for 1-66-month-olds, with questions assessing children’s abilities to undertake age-appropriate tasks. Summing items in each domain provides total scores (maximum 60) with higher scores indicating more optimal outcomes. The ASQ-3 has strong internal consistency reliability (82-.88), sensitivity (.86), specificity (.85) (Mackrides & Ryherd, 2011),and identifies children at risk for development problems (Lamsal et al., 2018) with age-appropriate cut-offs (i.e., delay) in each domain. Taking 10-15 minutes to complete, the ASQ-3 is typically administered in community agencies, thus both agencies and our pilot parents judged this measure acceptable and feasible.
Objective 1 Secondary Outcomes
Children’s Mental Health. We will employ the parent-report ASQ:SE (Squires et al., 2015) to assess newborn to 36-month-old children’s mental health. The ASQ:SE is suitable for 1-72-month-olds, with 30 items summed to assess social-emotional development, and lower scores indicating more optimal outcomes. The ASQ:SE exhibits good internal consistency reliability (.67-.91), sensitivity (.78), specificity (.84) (Squires et al., 2015), and provides age-appropriate cut-offs to indicate risk for mental health problems. Taking 10-15 minutes to complete, the ASQ:SE is typically administered in community agencies, thus both agencies and our pilot parents find these measures acceptable and feasible.
Parent-Child Relationship Quality and Attachment will be measured with the PCITS (Oxford & Finlay, 2013) and ATTACHTM Pre-school Attachment Screening tool (APAS) developed for this study. The PCITS (Oxford & Finlay, 2013) is an observational binary measure of relationship quality in an everyday teaching situation, designed for children 36 months or younger. Considered the gold standard for the assessment of parent-child relationship quality, PCITS consists of 73 items categorized into 6 subscales including parental sensitivity to cues, responsiveness to distress, cognitive growth fostering, and socio-emotional growth fostering, child clarity of cues and responsiveness to parent as well as parent total, child total, and parent-child total scores. Reliability and validity are well established (Letourneau et al., 2018)and was a strong measure of intervention impact in our pilot studies (Anis, Letourneau, et al., 2020; N. Letourneau et al., 2019).The observation typically takes 5 minutes and is video recorded to enhance the accuracy of data coding. ATTACH™ facilitators who are health care professionals in agencies will be trained to administer the video recordings via Zoom™. A robust Zoom data collection protocol was developed during the ATTACH™ Online pilot study for PCITS. Coders, reliable at 90th percentile with the University of Washington and who retained >95% intra-rater reliability over the course of pilot studies on 10% of recoded videos, will code all video recorded interactions. Coders are trained and supervised by PI Letourneau who has been a certified PCITS trainer since 1996 and has consistently maintained reliability in the delivery of the PCITS.
The ATTACHTM Pre-school Attachment Screening tool (APAS), designed to be used with children between 24 months – 60 months, is a tool developed to screen attachment behavior, based on coding a 5-minute free play session in which a primary caregiver (parent, guardian, or custodian) is asked to “frustrate” the child by removing the desired toy of interest from the child during a play session. Such frustration tasks are commonly used in studies that examine children’s emotion regulation [e.g., (e.g., Calkins et al., 2002; Calkins & Fox, 2002; Calkins & Johnson, 1998; Calkins et al., 1998; Goldsmith et al., 2008). During a 5-minute free play session, caregivers are instructed to ‘play with their child as they normally would’ for the first three minutes of the play session, and then after receiving a cue from the camera person (usually three tapping sounds made by tapping on the camera) the caregiver is signaled to remove and disallow the child from playing with a favored toy (by holding the item behind the caregiver’s back) for one minute to induce mild frustration in the child. Then after receiving another tapping cue from the camera person (usually three tapping sounds made by tapping on the camera) the caregiver is signaled to return the desired toy of interest to the child for the last minute of play.
Coders focus on the child’s response during the frustration portion of the play session and how the caregiver may (or may not) repair the breach in the dyadic play. The child’s response to this stressful event provides valuable information about the caregiver/child relationship and the child’s attachment pattern. Trained coders observe the child’s response then classify the child’s attachment pattern as either secure (Type B) or insecure (Type A, C, D) by using similar coding indices of established attachment measures, namely the MacArthur preschool attachment coding system (MAC) as taught by Dr. William Whelan (Anis, Ross, et al., 2022), which has been adapted for older preschool-aged children from Mary Ainsworth’s Infant Strange Situation Procedure (SSP) (Ainsworth et al., 1978). Thus, the MAC and SSP serve as the foundational model.
Parental RF. This will be assessed via the PRFQ (Rutherford et al., 2015) and is an 18-item measure, with subscales assessing: (1) pre-mentalizing (2) certainty about mental states, and (3) interest and curiosity about mental states. Higher scores indicate higher levels of parental RF. The PRFQ has good internal consistency (.7-.84) and takes 5 minutes to complete. Pilot testing revealed the PRFQ detected intervention impacts and was acceptable to parents. In our other work (Anis, Perez, et al., 2020), we show that scores on the PRFQ associate significantly (p<.05) with the gold standard Parental Development Interview (Slade et al., 2004)coded with Fonagy’s 11-point scale (Fonagy et al., 1998).Given the gold standard requires 1-2 hours per parent interview, followed by 1 hour to check automated transcriptions, and 3 hours of coding per interview (~6 hours total), the use of the PRFQ reduces parent burden, costs, and is feasible to implement in agencies.
Objective 2 Primary Outcomes
Implementation Fidelity Assessment
ATTACH Online Implementation fidelity will be assessed via a published, validated, ATTACH™ specific fidelity tool (Anis et al., 2021)that was developed to assess health care professionals’ adherence and delivery of key ATTACH™ intervention elements (i.e., video feedback of parent-child interactions, real life stressful and hypothetical situation reviews). ATTACH Online Implementation fidelity will be assessed more broadly by NPT interviews with parents, health care providers, and agency administrators by eliciting participants’ perceptions of facilitators and barriers to achieving fidelity of delivery of ATTACH™ Online elements and potential strategies to promote fidelity.
Objective 2 Secondary Outcomes
Uptake of ATTACH Online by agency clients will be quantified as a percentage score based on the number of families delivered ATTACHTM by trained service providers, divided by the number of eligible families in a given agency. NPT interviews will further determine participants’ perceptions of facilitators and barriers to uptake and potential strategies to promote uptake.
Participant Timeline {13}
Objective 1:
Pre-Intervention. ATTACH™ Online begins with collection of pre-intervention assessment data including observational and questionnaire sources.
ATTACH™ Online. The program begins after the pre-intervention sessions are completed–usually the following week. ATTACH™ Online sessions are described above in {11}:
Post-Intervention Phase. The ATTACH™ Online intervention must be complete before post-intervention assessment which includes parents’ providing observational and questionnaire data.
Delayed Post-Intervention. Three months after the post-intervention data collection is complete, parents will be reassessed, providing questionnaire data.
Objective 2: To describe implementation fidelity and uptake of the ATTACH™ Online intervention and to explore the mechanisms influencing these outcomes with respect to coherence, cognitive participation, collective action, and reflexive monitoring, recruitment for participation in NPT interviews will begin shortly after the first family completes the ATTACH™ Online program (likely in Spring, 2024). Recruitment will continue until data saturation is attained, i.e., the degree to which new data repeats or is redundant with what was expressed in previous data (Patton, 2002; Saunders et al., 2018). We will employ a stopping rule. Data collection in a category (parent, health care professional, and administrator) will cease when three interviews in a row offer less than 10% new information (i.e., only one question of the 13-15 interview guide questions offers new information).
Sample Size {14 including 14.1}
Objective 1:
Quantitative component. We will examine pre-intervention/post-intervention differences from the primary outcome of development, and our secondary outcomes of children’s mental health, parent-child relationship and attachment quality and parental RF with 100 parents and children (aged newborn to 36 months). We will recruit 100 families, to attain a sufficiently powered N of 80 families with complete data, assuming up to 20% incomplete data. This is based on power of .90, and two-tailed alpha (p<.05/3=.0167, given Bonferroni correction applied for separate comparisons using three developmental outcomes). Pilot data from the in-person ATTACH™ program tests revealed relevant effect sizes for child development, ranging from d=.44-.98 for communication, personal social, problem-solving skills (Anis, Letourneau, et al., 2020; Anis, Ross, et al., 2022; Letourneau et al., 2023). Thus, eighty complete participant family data sets will be sufficient to detect conservatively moderate effect sizes for within group differences (d=.44) for each of the three developmental outcomes (communication, personal-social, problem-solving) between pre-intervention and immediately post-intervention. Multiple discussions with agency knowledge users give confidence that it will be feasible to recruit an average of 8-10 families (including parents, co-parents, and children) from each agency from rosters of parents currently seeking service and to retain them for 3 months post-intervention for follow-up. Any longer was deemed unrealistic given potential for parent relocation.
Objective 2
ATTACH™ Online Implementation. From discussions with agency administrators, it will be feasible to recruit 20 parents, 20 health and social service providers, and 20 administrators (total n= 60) for interviews. However, recruitment and data collection will continue only until data saturation (Anis, Letourneau, et al., 2020; Straus & Douglas, 2004).
Recruitment {15}
Objective 1:
ATTACHTMOnline Effectiveness. Every partner agency will recruit 2-5 staff members for ATTACH™ Online training to become the ATTACH™ Facilitators. To partake in ATTACH™ Online, participants will be identified through partner agencies. We will recruit up to 100 parents and their newborn to 36-month-old children to retain 80 complete pre- and post-intervention data from approximately eight Alberta agencies. Parents will be recruited from rosters of parents currently seeking services at these agencies. ATTACHTM Online information sheets and brochures will be posted on agency implementation sites. Agency staff will assist with recruitment as participants seek their services in routine care.
Objective 2:
ATTACHTM Online Implementation. Parents,health and social service providers, and administrators from each of the 10 agencies will be recruited via convenience sampling methods.
Methods: Data Collection, Data Management, Statistical Methods, Monitoring, and Analysis
Data collection methods {18a (18a.1, 18a.2) 18b}
Objective 1: ATTACH™ Online Effectiveness. Knowledge users at agencies and researchers agreed to reduce parent burden from data collection. Thus, demographic data will be obtained from agency administrative records as much as possible, e.g., ethnicity, sex, gender, first language, marital status, education, employment, number of children, and age (parents and children) at baseline. To further reduce burden, many measures have been selected from intake data collection already conducted in agencies, e.g., ASQ-3 (Bricker & Squires, 2009). We will include covariate measures of adversities that are often administered at parent intake for: (1) Depressive symptoms with the Edinburgh Depression Scale (EDS) (Cox et al., 1987; Matthey et al., 2006),a 10-item self-report tool to measure depression with sensitivity of 66.7-69% and specificity of 67.7% that takes 5 minutes to administer, (2) Family violence with the Revised Conflict Tactics Scale-Short Form (CTS2-SF) (Straus & Douglas, 2004), a 20-item questionnaire with internal consistency of .79-.95 that takes 3 minutes to complete, and (3) Parents’ adverse childhood experiences with the Adverse Childhood Experiences (ACE) (Felitti & Anda, 2009)Questionnaire, consisting of 10 questions, with extensive reliability and validity data that takes less than 3 minutes to complete. To assess the covariate of parent strengths in the face of adversity, the Brief Resilience Scale (BRS) (Smith et al., 2008)will also be administered, a 6-item tool with internal consistency ranging from .80-.91 that takes 3 minutes to complete. All questionnaire data will be collected at baseline, immediately post-intervention, and 3 months post-intervention by agency health care professionals/ATTACH™ facilitators, who will be trained and supervised to collect questionnaire data via REDCap (www.project-redcap.org) using iPads provided during the ATTACH™ training.
Objective 2: ATTACH™ Online Implementation. Basic demographic data will be collected from knowledge users, including age, sex, gender, employment, and education. Fidelity will be assessed via the published, validated, ATTACH™-specific fidelity tool (Anis et al., 2021)completed by health care professionals after every ATTACH™ interaction with parents. Uptake-relevant data will be collected from agency administrators via a brief survey including their demographic information. NPT interviews will further examine implementation fidelity and uptake and mechanisms to promote more optimal delivery of ATTACH™ Online. These will begin shortly after the initially enrolled parents complete the intervention and continue until data saturation. An NPT-guided interview was created to assess implementation and finalized with input from knowledge users engaged in review, feedback and decision making and pilot tested before use. Interviews will be digitally audio recorded with Zoom (Graucher et al., 2022) and automatically transcribed verbatim with Otter.ai (Lee et al., 2022; Mahdi, 2021),and checked for accuracy, with privacy protections in place to guard participant identity and personal information.
Data Management {19}
Partner agencies will collect the data via iPads with REDCap software installed, as per best practice recommendations (Garcia & Abrahão, 2021; Komanchuk et al., 2023; Rivera et al., 2021).Agency health and social service providers/ATTACH™ Online Facilitators will be trained and supervised to employ the iPads and REDCap as part of the ATTACH™ Online Training Program. Partner agency health and social service providers/ATTACHTMOnline facilitators will be provided with a login information to access the baseline, immediate post-intervention, and delayed post-intervention questionnaires. After logging in, Facilitators will ask the participant to fill out the questionnaires, which will only request de-identified data (except for required linkage to consent, filed separately); data will be automatically shared to the REDCapwebsite after completion. Any data sharing or communication from the partner agencies will be done via the University of Calgary domain specific email account. Digital video data will be saved on the iPads and uploaded to secure Box on the cloud (https://www.box.com/en-ca/capture). The staff at the local agencies will be trained to delete any digital data from the iPads. Digital copies of transcripts and audio files will be kept in a secure network location administered by the University of Calgary’s Information Technology services and accessible only to the research team.
All the information contained in our analyses and summaries will be anonymous and based on group data. Published reports will not identify participants by name, address, agency, or any other personal information. Furthermore, all research team members are aware of the importance of maintaining participant anonymity and are required to sign a confidentiality agreement.
Statistical Methods {20a (20a.1), 20b and 20c}
We will analyze the demographic characteristics of the sample with measures of central tendency and frequencies as appropriate. Alpha will be set a priori at .05 (two-tailed) unless testing directional hypothesis (one-tailed).
Objective 1: ATTACHTMOnline Effectiveness. For(1a), to evaluate ATTACHTM Online program effects on children’s development (primary outcome), children’s mental health, parent-child relationship and attachment quality, and parental RF (secondary outcomes) immediately post-intervention and at 3 months post-intervention, we will employ repeated measures analysis of variance (ANOVA), paired-t-tests, and chi-square tests to examine outcomes between baseline, immediate post-intervention, and delayed post-intervention assessments. We will undertake three sets of analyses for our primary hypotheses tests. For (1b) to determine whether ATTACHTM Online is equally effective across parent populations (and for whom it works best/worst), we will examine differences among sub-groups derived from known covariates through use of independent samples t-tests (two groups, e.g., child sex), ANOVAs (more than 2 groups, e.g., race/ethnicity), repeated measures analysis of covariance (with identified covariate) and linear regression models (continuous covariate, e.g., age, years of education).
Additionally, we will consider child sex as a covariate and stratification variable in our analyses. We will include both mothers and fathers in the ATTACHTM Online implementation and examine impacts on parents as a group, with separate analyses for mothers and fathers, even though fathers are likely to be far fewer in number than mothers. (One of our partner agencies serves many fathers). We will also consider gender in our analyses. Parents will report the gender that they identify with, preferred pronoun, and preferred term for themselves as a parent, e.g. mother, father, or another word. While insufficient numbers will likely limit interpretability, we will consider parents’ characterizations as cis-, trans-gender, or gender-diverse in analyses. For children, while it is unlikely that preschoolers will be non cis-gender, we will consider parent-reported child gender in our analyses, to the degree possible. These analyses will help determine how the ATTACHTM Online may affect different sex and gender-based patient populations.
Objective 2: ATTACHTM OnlineImplementation. The fidelity assessment tool will be quantified by evaluating adherence to program content elements; each element is coded as Yes (attempted= implemented as intended) or No (not attempted = never asked or failed to perform) (Anis et al., 2021). To be considered satisfactory, content fidelity is expected to be 90% or higher for Yes category, or 10–20% or lower for No category (Anis et al., 2021). After all participants have been recruited, uptake data will be calculated with scores applied to each agency. Data on variables such as health care professionals’ years of experience, age, gender will be collected and considered for their impacts on fidelity and uptake. Qualitative analysis of NPT interviews will involve the stages of thematic analysis including familiarization, coding, theme development, and data reporting (Terry et al., 2017). Theme and sub-theme development will be deductive, using a priori codes dictated by interview questions to explain factors that promote or inhibit the intervention from being embedded in agency practice. Two trainees will code the data, supervised by PI Letourneau, who is experienced in qualitative data analysis. Coding will inform when data saturation is reached. Data will be managed with Dedoose (Sociocultural Research Consultants, 2021). Data from parents, service providers, and administrators will be coded separately, and coding trees examined for similarities and differences post-hoc. Once themes and sub-themes are finalized, findings summarized in draft reports will be shared with key informants as a validation check (Richards, 2005). Data from parents, service providers, and administrators will be coded separately, and coding trees examined for similarities and differences post-hoc.
Methods: Monitoring
Data Monitoring {21a, 21b}
Because this is a social intervention, not a drug or pharmaceutical trial, there is no data monitoring committee or interim analysis (Anis, Letourneau, et al., 2022).
Harms {22}
Observed incidents such as mental health crises, will be documented and managed as necessary by agency personnel delivering ATTACH™ Online (e.g., by providing appropriate comfort measures as well as mental health referrals). It is important to note that ATTACH™ facilitators are also employees of health and social service agencies who serve the clients/participants. If the investigators or ATTACH™ facilitators interacting with these families observe child abuse, they will report it to the Law Enforcement Authorities, as is required by law.
Auditing {23}
As ATTACHTM is a social intervention rather than a drug or pharmaceutical trial, there is no data auditing (Anis, Letourneau, et al., 2022).
Ethics and Dissemination
Research Ethics Approval and Consent or Assent {24 and 26a}
Ethics approval has been obtained from the Conjoint Health Research Ethics Board (CHREB; Ethics ID: REB20-0903) of the University of Calgary, and all participants will undergo a process seeking their informed consent. The University of Calgary is the lead agency conducting this study and partner agency research sites rely on CHREB’s approval as part of their agency ethics protocols. All funding and research guidance flows from the University of Calgary and while partner agencies will typically not have access to the study data, nor have direct involvement in data analysis or data storage, some knowledge users involved in the project may become more involved, requiring their addition to the ethics file as needed with all appropriate safeguards for participant safety, anonymity, and confidentiality maintained. All participants will be asked to provide informed consent. The process of informed consent involves verbal consent secured at each stage of the process, including recruitment, screening, intervention, and data collection. Participants will be provided with an electronic consent form for their signature. This will be retained by the study investigators and participants will receive a signed copy. We have created different consent forms for the and intervention participation and individual interviews to clearly indicate to what participants are consenting (see Appendix 1; Appendix 2).
The voluntary nature of the study will be reinforced verbally throughout the consent process and, indeed, throughout the course of the participants’ involvement in the study data collection. They may choose not to answer some questions, or to withdraw from the study at any time without affecting their receipt of the ATTACH™ Online program, health care or other partner agencies’ services. If they choose to no longer participate (at any time including once data analysis has begun), we will retain their data for attrition analyses, unless asked explicitly to remove data from the study, in which case we will attain the participants’ unique numeric identification (see below, Confidentiality) and delete all relevant data. Staff at the participating agencies will avoid any coercion by letting the potentially interested families know that their participation is completely voluntary, and that they can withdraw any time. Access to agency services will not be affected by participation or withdrawal.
Ethics approval has been received for an adaptive honorarium schedule of gift cards that provides increased compensation commensurate with increased parent burden. This schedule emerged from numerous collaborative conversations with parents and agency health and social service administrators and providers. Study participants will be offered $100.00 in Amazon gift cards in increasing value over 10 sessions. Moreover, each NPT interviewee will be given a $30 gift card, in compensation for a 60–90-minute NPT interview.
Protocol amendments {25}
There have been no amendments to the protocol.
Consent or assent {26b}
In ancillary studies, participants' data and biological specimens are not subject to additional consent provisions.
Confidentiality {27}
All data will be held confidentially and stored on a secure network drive. To ensure anonymity, participants will be assigned unique numeric codes in place of names. There will be no use of personal email accounts or emails for communication or for sharing of data. To ensure that participants understand the privacy and confidentiality nature of the study, the staff will ensure that they sign the consent form at the beginning of the study. Additional steps may include reiterating the privacy and confidentiality nature of the study before initiating the video recording.
The partner agencies will collect demographic information about parents, such as their name and age. Apart from the consent form (stored separately), partner agencies will only share de-identified data associated with participants’ unique numeric codes, with the ATTACHTM Online Team. The demographic information will be used to describe our sample in our future publications. The interactions between the parents and children will be video recorded for the purpose of assessing the quality of parent-child interaction and attachment. These assessments are based on age and any video data that is digital will be password protected and encrypted. Participants will only be identified by an ID number, so researchers will not have access to any identifying information. Any identifying information will be removed from the beginning and replaced with an ID number for analysis. Only the research team will have access to questionnaire response data. All information provided by participants will be kept confidential, except when it needs to be reported as required by law (such as when participants express a desire to do harm to themselves or others). Participants will not be identified in any publications or presentations that result from this research. The findings will be presented at health conferences and published in scientific journals as aggregate data. Any information that could identify participants will not be included.
Declaration of interests {28}
No competing interests are declared by the authors.
Access to data {29}
Data used and/or analyzed during this study may be made available by the corresponding author upon request and in compliance with the University of Calgary and ATTACHTM Online program research collaboration and data transfer guidelines.
Dissemination policy {31a, 31b, 31c}
Our team including researchers and the Community Engagement Committee members, will generate an array of dissemination products, including traditional high-impact peer-reviewed papers and presentations as well as innovative products such as in-services, infographics, and opinion-editorials. Principal knowledge user Reimer will share progress/findings in the network of Women’s Shelters in Alberta, promoting widespread ATTACHTM Online program uptake. We will continue our ongoing ATTACH™ webinar series (see https://attach.teachable.com/ p/webinar-series), sharing progress and emerging findings with a wide audience. Publications will adhere to CIHR’s open access policy (http://www.cihr-irsc.gc.ca/e/46068.html) as well as CIHR’s sex and gender-based analysis policy (http://www.cihr-irsc.gc.ca/e/ 50833.html). Reporting guidelines will be employed in published papers, e.g., Consolidated Standards of Reporting Trials (CONSORT) (Antes, 2010; Schulz et al., 2010), Template for Intervention Description and Replication (TIDieR) checklist (Hoffmann et al., 2014), GRIPP-2SF (Preston et al., 2023; Staniszewska et al., 2017), and Consolidated Criteria for Reporting Qualitative (COREQ) (Tong et al., 2007) research.