Study setting
This analysis uses data collected as part of a randomized control trial of GC-CCP in Eastern Uganda between September 2021 and April 2022. The pilot study was conducted at Buyinja Health Center IV and Banda Health Center III in Namayingo, a rural community in the Busoga region of Uganda. The selection of the study site was influenced by previous work in this area by our partner institution (Rays of Hope Hospice Jinja; RHHJ) coupled with low CC screening rates observed among women in this district. CC screening and thermal therapy are available at both Buyinja and Banda health centers, and from RHHJ which conducts periodic mobile CC screening and thermal therapy “day camps”. Women who need biopsies are sent to Jinja (approximately 90 km from Namayingo), and if cancerous lesions are present, they are referred to the Uganda Cancer Institute, the leading tertiary public cancer care centre located in Kampala.
Study design
The study design has been described in detail in our previous publication (Wanyenze et al., under review). In brief, women who had recently screened for CC (referred to as index participants) were randomized to receive the GC-CCP intervention (intervention arm) or assigned to the wait-list control group, with individual randomization on a 1:1 ratio. Women randomized to the wait-list control group received the intervention after data collection was completed. Randomization was stratified by age (under and over age 35) and history of CC-related treatment. Participants were not blinded to assignment; only the data analyst was blinded. Each index participant was asked to enroll up to three women in their social network (referred to here as “alters”) who had not screened for CC in the past 3 years (though all alters reported never having been screened). All participants (index and alter) were administered assessments at baseline and month 6, and received 30,000 Uganda shillings (~$8 USD) for each completed assessment. The primary outcome was alter CC screening over the 6-month follow-up period. The trial was registered on ClinicalTrials.gov (NCT04960748) on 14/07/2021.
Participants
Index participants were enrolled into the study if they were aged 18 years or older, had screened for CC within the past year, had stable health status (i.e., not in end stages of disease, so that they were likely to complete the 6-month study follow-up), and had shared their CC screening experience with at least one woman (alter) who they perceived to not have screened for CC in the past 3 years. Alter participants were eligible if they were at least 18 years of age, were recruited by a woman who was enrolled as an index participant, and self-reported not being screened for CC in the past 3 years. All participants had to speak either Samia or Lusoga, the two prominent languages in Namayingo district.
Recruitment of index participants was purposive in order to recruit a balance of women who screened positive for signs of CC risk (pre-cancerous or cancerous lesions), and women who screened negative, so that we could assess whether this factor was associated with the outcomes measure of engagement in CC prevention advocacy. Candidates for index participation were informed of the study by health care providers and those who expressed interest were referred to the study coordinator for confirmation of eligibility and consent procedures. Women who decided to enroll were administered the baseline survey, which included listing up to 12 women in their social network. To recruit alters, we randomly selected five alters who the index participant reported as knowing her CC screening experience (or as many as there were if less than five); the index participant was then asked if she was comfortable asking three of these alters to participate. The index participant was asked to call each selected alter at the end of the interview to describe the study in the presence of the coordinator, who then scheduled a study visit if the alter expressed interest in participating. If an alter refused or could not be reached, a replacement was randomly selected from the list of alters who knew the index participant’s CC screening experience (and whom the index participant was comfortable recruiting). When screening the alter, the coordinator confirmed that the individual was not already recruited by another index. All participants provided written informed consent.
Intervention
The intervention has been described previously (Wanyenze et al., under review). In brief, the intervention consisted of seven weekly group sessions. Session 1 focused on addressing fears and concerns related to CC risk and use of self-compassion and peer support to overcome fears and internalized stigma, as well as introducing the overall vision for empowering women to become change agents for CC prevention and treatment. Session 2 focused on building skills and decision making for sharing one’s personal CC screening experience, knowing to whom to disclose and when, and how to initiate and navigate disclosure and conversations about CC. Session 3 built skills and motivation for recognizing signs of CC risk and seeking health services, so that the advocate’s own behavior was consistent with the behavior they encouraged in others, as well as instruction on facts and myths related to CC to facilitate accurate CC screening advocacy. Session 4 introduced the concept of a social network and how one’s network can serve as a tool for CC prevention advocacy and dissemination of CC-related information. Sessions 5 and 6 focused on the skills needed for successful CC prevention advocacy, including strategies for how to start and sustain conversations about CC, and effective communication skills (e.g., reflective listening, paraphrasing, open-ended questions). Session 7 focused on peer solidarity and support to inspire a commitment to ongoing CC advocacy. The sessions were administered in a group format to facilitate the use of: sharing of experiences to build support, solidarity and motivation among participants; group problem solving and role playing to build skills and self-efficacy; setting personal goals regarding disclosure and advocacy; and take home activities to reinforce practice of new skills and generate personal experiences to be processed in the sessions. Each session lasted 120–150 minutes.
The sessions were conducted using a structured facilitator manual, in the predominant local languages of Samia and Lusoga, by two peer facilitators from Namayingo who themselves had been screened for CC. The facilitators were trained by the senior investigators over three days. The supervisor of the facilitators observed the implementation of each session and provided feedback and further training as needed during weekly supervision.
Measures
Assessments included a standard survey (index and alter participants) and social network assessment (index participant only), which were administered in either Samia or Lusoga (depending on the preference of the participant) using Network Canvas computer-assisted software. Each measure was assessed with both index and alter participants, unless otherwise noted. Measures were translated using standard translation/backtranslation methodology. CC screening and treatment utilization were verified with abstracted medical chart data. All measures were developed by the study team, except those in which an attribution is cited. For measures developed by the study team that included at least three items, we cite internal reliability statistics (Cronbach’s alpha).
CC screening and treatment. Data were collected to determine if the participant had ever been screened for CC using visual inspection using acetic acid (VIA) or pap smear, and if so, when. For participants who had been screened, it was determined if the screening resulted in pre-cancerous lesions or potential cancerous lesions, in separate items; if either type of lesion was reported, receipt of corresponding procedure or treatment (cryotherapy or thermal therapy for pre-cancerous; biopsy to confirm diagnosis, and radiation, chemotherapy or surgery treatment for cancerous) was assessed.
Potential mediators. The following measures were assessed as potential mediators of the effects of intervention effect on alter CC screening, as each was targeted by the components of the intervention. Internalized CC stigma was assessed among index participants, using 5 items adapted from a scale of HIV internalized stigma (e.g., “My cervical cancer screening makes me feel ashamed of myself” [15]); higher mean score reflects greater stigma. Sharing of CC screening experience was assessed by asking respondents to what extent they had shared their CC screening result with sexual partners, family, and friends, in separate questions; higher mean item score reflects greater disclosure (Cronbach’s alpha = .74). CC knowledge was assessed with 16 statements or questions reflecting the etiology, prevention and treatment of CC; a sum of correct responses was calculated. Internal reliability was moderate (Cronbach’s alpha = .75). CC enacted stigma was assessed among alter participants with six items adapted from measures developed by Marlow & Wardle [16] and Cho et al. [17]. Participants were asked to rate their agreement with statements (e.g., A woman with cervical cancer is to blame for her condition; I feel uncomfortable when I am around women with cervical cancer) by indicating they 1 ‘disagree’, 2 ‘I neither agree nor disagree. I do not have a feeling either way’ or 3 ‘agree’; mean item score was calculated and higher scores reflect greater stigma. CC risk management self-efficacy was assessed with three items that measured confidence to notice a symptom of CC risk, seek health services for a symptom of CC risk, and obtain treatment if screening revealed signs of CC risk; higher mean item score reflects greater self-efficacy. Internal reliability was low (Cronbach’s alpha = .64). CC prevention advocacy self-efficacy was assessed with three items assessing confidence to start a conversation about the need for: CC screening, treatment for signs of CC risk, and telling someone about their CC screening experience; higher mean item score reflects greater self-efficacy (Cronbach’s alpha = .85). CC prevention advocacy was assessed with six items in which respondents with the reported frequency of discussing CC-related topics (e.g., importance of CC screening, how and where to get screened, importance of getting treatment if signs of CC risk are present) with women they know in the past six months. Response options ranged from 1 ‘not at all’ to 5 ‘very much’; mean item scores were calculated and higher scores reflect greater engagement in advocacy. Internal reliability was high (Cronbach’s alpha = .95).
Potential moderators. The variables we examined as potential moderators among both index and alter participants consisted of age and any secondary education, in addition to CC-related treatment history (index participants only) and presence of a main sex partner (alter participants only).
Data Analysis
Descriptive and bivariate (2-tailed independent t-tests; chi-square tests) statistics were used to compare baseline sample characteristics of index and alter participants in the control versus intervention arms, in separate analyses. To examine intervention effects on index and alter measures of CC-related processes, we conducted multiple linear regression analyses. In each model, the month 6 measure of the outcome was the dependent variable, while independent variables included the baseline measure of the dependent variable and an indicator of study arm. If a measure was missing at month 6, the baseline measure of the variable was used to replace the missing value. Similar models were run to examine whether alter uptake of CC screening by month 6 was associated with the index and alter measures of CC-related processes.
Measures of index and alter CC-related processes (potential mediators) were examined as mediators of the intervention effect on alter uptake of CC screening if the measure was significantly associated with both the intervention and alter CC screening. To test for mediation, we employed Proc Causalmed (SAS v9.4), which uses bootstrap resampling to compute standard errors and confidence intervals for causal mediation effects and decompositions. A two-step approach was used to test each potential mediator separately. In step one, the dependent variable was alter uptake of CC screening by month 6, while independent variables consisted of an indicator of study arm and the baseline measure of the mediator. In step two, the month 6 measure of the mediator was added to the model, resulting in the model assessing the mediating effect of change in the mediator from baseline to month 6. Covariates included in each model consisted of age < 35 years, any secondary education, and presence of a main sex partner. We examined each potential mediator separately, because the mediators are conceptually inter-correlated, and testing multiple mediators simultaneously would complicate the interpretation of the models. To test for moderation of the intervention effect on alter CC screening, for each potential moderator we ran a logistic regression modeling alter CC screening at month 6 as the dependent variable. Independent variables included an indicator for study arm, the moderator measured at baseline, and their interaction.
Ethical considerations
The study protocol was reviewed and approved by the Makerere University School of Public Health Research and Ethics Committee, and the Uganda National Council for Science and Technology.