Patient and Public Involvement
No patient involved.
Study design
This study is a randomized, single-blind, wait-list controlled, parallel-arm trial. Elderly stroke survivors will be selected from a tertiary hospital in China using convenience sampling between December 2022 to March 2023. Elderly stroke survivors who meet the inclusion criteria will be informed of the purpose and methods of the study and sign the informed consent forms through face-to-face communication. Then, they will be randomly assigned to either a wait-list control group (TAU group) or an intervention group (group-based ACT group). EA, PSD, psychological distress and quality of life of patients will be blindly evaluated at baseline (T0), post-treatment (T1), one-month follow up (T2) for both groups (see Fig. 1).
Through literature review, qualitative interviews and group discussions, this study established an initial intervention program of group-based ACT for elderly stroke survivors. Two rounds of Delphi expert consultations were conducted on the group-based ACT program via email for initial intervention program. The recovery rates of expert questionnaires in the two rounds were 70% and 100%, respectively, with Ca standing at 0.95, Cs at 0.87 and Cr at 0.91, indicating that the authority of experts was high and the reliability of consultation results was effectively guaranteed. The Kendall’s W coefficients of the two rounds were 0.130 and 0.126 respectively (P < 0.05), and the experts’ opinions tended to be consistent.
According to the expert opinions and the characteristics of elderly stroke, the intervention program was adjusted as follows: elderly stroke patients were prone to coughing and choking when eating raisins in the traditional mindful diet, so the program was adjusted to sour date cake or chocolate; in the preliminary experiment, the elderly did not accept the metaphorical animation of “Monster on the bus” quite well, and considered it childish, so it was changed to a video or other game. In addition, in the intervention program, other members of the group-based ACT intervention team would assist in completing the game, considering if the elderly had physical impairment.
Eligibility criteria
Inclusion criteria are: (1) conforming to the World Health Organization diagnostic criteria of stroke and confirmed by magnetic resonance imaging (MRI) or computed tomography (CT); (2) age ≥ 60 years old; (3) disease duration of more than half a year and having passed the acute stage and standard treatment; (4) reporting a clinically significant level of psychological distress (Hamilton Depression Scale scored ≥ 8); (5) having the ability to communicate on a daily basis; (6) agreeing to participate and provide informed consent; and (7) having the ability to use WeChat.
Exclusion criteria are: (1) having other organic encephalopathy such as respiratory, cardiovascular, digestive and other serious physiological diseases; (2) having a history of alcohol or other psychoactive substance abuse or dependence; (3) having dementia, a recognized complication of stroke; (4) limb function weakened, and could not tolerate sitting for one hour.
Sample size calculation
The sample size estimation formula of the mean of the two groups is adopted for calculation: N1 and N2 are the required sample contents; σ is the population standard deviation; δ = µ1-µ2, that is the difference between the two population means; The α is the type Ⅰ error probability, i.e. the test level or significance level, which is 0.05 on both sides in this study, \({u}_{\alpha }\) is 1.96. The β is class Ⅱ error, which is 0.1, \({u}_{\beta }\) is 1.282.
$${n}_{1}={n}_{2}=2{\left[\frac{\left({u}_{\alpha }+{u}_{\beta }\right)}{\delta /\sigma }\right]}^{2}+\frac{1}{4}{{u}_{\alpha }}^{2}$$
According to the above formula, the sample size of each group was about 25 cases. Taking into account the sample loss and other problems, each group was expanded by 30%. Therefore, the final sample size for each group was approximately 33 cases, a total of 66 cases were required.
Randomization
Randomization is performed by an independent researcher. Patients who volunteered for the study were numbered in the order of their admission. Sixty-six random numbers were generated using IBM SPSS Statistics for Windows (Version 26.0 Armonk, NY: IBM Corp) in descending order. Digits 1st through 33rd of the random-number sequence were numbered as the wait-list control group, and the remaining digits 34th through 66th were numbered as the intervention group.
Interventions
Wait-list control group
The wait-list control group will receive TAU treatment for eight weeks, and when the intervention group has completed all the ACT procedures, the wait-list control group will receive the same ACT intervention as the intervention group. The TAU intervention is as follows. (1) Disease knowledge guidance, including introducing to patients the causes of stroke, how to identify stroke, clinical manifestations, treatment methods and other knowledge, so that patients can have a more comprehensive understanding of stroke; (2) Medication guidance and health education, including the mode of medication, time of medication, precautions for medication, possible side effects after medication and how to deal with them; (3) Basic psychological guidance, including counseling, persuasion and other forms, enabling patients to feel respect and care, increase their trust in medical staff, and rebuild their confidence to resume normal life; (4) Rehabilitation guidance, including rehabilitation training timing, rehabilitation training methods and precautions; (5) Psychological nursing, including encouraging patients, timely answering their doubts in the process of rehabilitation treatment, reducing their fear of disease, and establishing their confidence in early recovery.
Intervention group
All interventions received by the intervention group were carried out in a separate activity room with an area of 20m3 to ensure no interference. The activity room will be equipped with 20 seats approximately, drinking water, and other necessary items. Moreover, necessary first-aid items will be also provided to ensure patient safety. The research team will provide materials and related things for ACT. Throughout the intervention, the health care workers will keep the patient safe at all times, and the family member or caregiver will also be fully involved in the entire intervention process.
For the intervention group, group-based acceptance and commitment therapy intervention will be given for 8 weeks in addition to TAU, which will be completed by 2 graduate students, both of whom were systematically trained group-based ACT consultants, and will also lead the group consultation activities. Each group-based ACT intervention will consist of 10 ~ 12 people, once a week for 40 to 60 minutes, for 8 consecutive weeks. The content consists of eight sessions: confronting the agenda, accepting everything, objectively observing cognition, hours, feeling yourself, identifying your value, looking forward, and review. See Table 1.
Table 1
An overview of the group-based ACT program for elderly stroke survivors
Session | Content |
Confronting the Agenda | Start with an "ice-breaking tour" (5–10 min) Patient self-introduction (10–15 min) Introduction of ACT team members and content (5 min) Mindfulness exercises (10–15 min) Home task (5 min) |
Accepting everything (Acceptance) | Begin with a mindfulness exercise and homework review (5–10 min); Watch the video "Swamp"(10-15min); Play the game "Chinese Finger Glove" (10–15 min); Share and summarize (10–15 min); Home task (5 min). |
Observing cognition objectively (Cognitive Defusion) | Homework review (5–10 min); Play the video "Monster on the Bus" (5–10 min); Play the game "Folder push" (10 to 15 min); Share and summarize (10–15 min); Home task (5 min). |
The Hours (Being Present) | Begin with a review of last week's homework (5-10min); Mindful eating (10 min); Mindful breathing exercise (10-15min); Share and summarize this activity (5–10 min); Home task (5 min). |
Feeling yourself (Self as Context) | Begin with a mindfulness exercise and homework review (5-10min); Play the video "Sky and Weather" (5min); Share and summarize (15-20min); Share poems, stories or elements of Chinese culture with the patients (5–10 min); Home task (5 min). |
Identifying your value (Values) | Start with a few people sharing thoughts on last week's homework (5–10 minutes); Play the game "Life Button" : (15-20min); Share and summarize (5-10min); Home task (5min). |
Looking forward (Committed Action) | Start with a few people sharing thoughts on last week's homework(10-15min); Set goals (20–25 min); Share and summarize (5–10 min); Home task (5 min). |
Review | Start with homework review (5 min); Play photos and videos (5–10 minutes); Share feelings (15-20min); Give blessings, encouragement, and gifts (10–15 minutes). |
Blinding
The researcher conducting baseline assessments (T0) will be blinded to participant treatment allocation, as participants will also be blinded to randomization after the baseline assessment (T0). It is not possible for the treating psychologists providing the intervention to be blinded. However, an independent assessor who will join to complete the post-treatment (T1) and one-month follow up assessment (T2), will be blinded to the condition. The success of blinding will be assessed by having independent assessors (i) indicate which condition they thought the participant will be randomly assigned to and (ii) indicate whether the participant will disclose their treatment condition or not. Data analysis will be undertaken by a graduate student with no direct contact with the individual research group to remain blinded to the treatment conditions. It is expected that unblinding will be not needed for independent assessors or statisticians, therefore in this study, unblinding is not permissible.
Quality Control
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The therapist will post reminders and trailers in the WeChat group before each intervention.
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The therapist will summarize and comment on the day after each session.
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The therapist will clock in the WeChat group to supervise the completion of the homework of the patients, and provide comments and feedback to the patients who actively share the experience after the completion of the homework. Patients can also communicate with each other in the Wechat group.
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Considering the declining vision and cognitive ability of the elderly, large-sized intervention explanatory sheets will be distributed in this study, and each patient will be provided with a helper to understand the intervention content.
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If required, the measures can be read out to the participant by the assessor to assist with understanding, and a separate sheet with the measure’s Likert response scales will be provided to the participant in a larger font to compensate for visual, attention/cognitive, and reading impairments in the elderly.
Statistical Analysis
The statistical analysis of this study can be divided into four parts. Firstly, the IBM SPSS Statistics for Windows (Version 26.0 Armonk, NY: IBM Corp) would be used in this study. Data processing was performed to review missing data, followed by screening for normality for all outcome measures and for each treatment group. Secondly, inter-group comparisons were performed prior to the main analysis, and differences between baseline groups were analyzed using Chi-square test and independent sample T-test to verify the success of randomization. If the relevant data did not conform to a normal distribution, the generalized estimation equation (GEE) would be used for analysis. In addition, a preliminary analysis would be performed on an intention-to-treat basis using Generalized linear mixed model (GLMM) to investigate the differential effects of each treatment condition. For the post-treatment analysis in the three treatment conditions, the analysis will focus on the linear time effect, treatment conditions and interaction. Finally, a linear mixed model repeated measures (MMRM) was used to study inter-group differences with primary and secondary outcome measures as dependent variables. The model would include processing conditions and time as classification variables, as well as their interaction effects. The baseline adjusted mean difference between groups at each time point would be calculated using a 95% confidence interval, with the value of alpha set at 0.05. The analysis would focus on the estimated mean differences between primary and secondary outcome indicators at different time points.
Primary Outcome Measures
The Acceptance and Action Questionnaire-Ⅱ, AAQ-Ⅱ
AAQ-Ⅱ scale, a seven-item questionnaire developed by Bond et al. (27) in 2011, was used to assess EA. In the questionnaire, items are scored on a 7-point Likert scale with a total score ranging from 0 to 49, and a higher score indicating more EA. The internal consistency of the AAQ-II is good (Cronbach α = 0.84)(27). In 2013, Yao et al.(28) measured the reliability of Chinese version of Acceptance and Action Questionnaire-II (AAQ-II), which consists of 10 items rated on a Likert scale of 1 ~ 7 points. The score for items 2 ~ 5 and 7 ~ 9 is reversed. The total possible score ranges from 10 to 70, with higher scores representing higher levels of general acceptance. The coefficient of Cronbach’s α for the Chinese version was 0.705, and the standardized item alpha was 0.758, indicating a good internal consistency of the questionnaire.
Secondary Outcome Measures
The Hamilton Depression Scale, HAM-D
The HAM-D scale, developed by Hamilton(29) in 1960, is the most commonly used scale to assess post-stroke depression. The revised 24 Chinese HAMD items is also used in this study. A total of 24 items are divided into 7 dimensions: anxiety/somatization (6 items), body quality (1 item), cognitive impairment (6 items), day-night changes (1 item), sluggishness (4 items), sleep disorders (3 items), and feelings of hopelessness (3 items). The scale was scored using the likert 5 rating method (no = 0, mild = 1 minute, moderate = 2 points, and severe = 3 points, heavy = 4). The total score of the scale ranged from 0 to 76, with > 35 being classified as severe depression, 21–35 as mild to moderate depression, 8–20 as possible depression, and < 8 as no depression(30). The Cronbach's α coefficient of the Chinese version of the HAMD-6 was 0.91, and the intra-group correlation coefficient (ICC) for retest reliability was 0.81(31)
Distress Thermometer, DT
Developed by Gilson(32), DT could reflect the patient's psychological distress level during the past week. The scale consists of two parts: (1) DT, a scale of 0 ~ 10 points (0: no pain, 10: extreme pain), with higher scores representing more severe psychological distress of the patient. (2) The 39-question list is a list of questions related to psychological pain examined by the patients, with a total of 6 dimensions and 39 items. In this study, only the psychological pain thermometer score was used and it was divided into three levels: 0 ~ 3 for mild; 4 ~ 6 for moderate, and 7 ~ 10 for severe. The Cronbach's α coefficient of this scale was 0.808, which has good reliability and validity.
Stroke-Specific Quality of Life, SS-QOL
SS-QOL, developed by Williams et al(33), is used to assess the quality of life. It is a reliable and effective tool for measuring health-related quality of life in Chinese stroke survivors(34). The scale consists of 11 domains (47 items), including activities, mood, energy and family roles, language, upper extremity function, relationships, thinking, vision, basic needs, personality, leisure and work, and transfer, each with a score of 1 ~ 5 points. The internal consistency of SSQL-C is high. Cronbach’s alpha for the total scale was 0.93, and Cronbach’s alpha for all 11 domains ranged from 0.63 to 0.90(34).