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Completed

NCT Number: NCT06042634

A Feasibility Study of Online Psychoeducation for Family Caregivers of People With Dementia

The goal of this clinical trial is to evaluate the feasibility and acceptability of online psychoeducation in the family caregivers of people with dementia living in the community. The main objectives it aims to answer are:

1. Is online psychoeducation feasible and acceptable to family caregivers of people with dementia? 2. What is the preliminary effect of online psychoeducation on caregiving self-efficacy in family caregivers of people with dementia?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nethersole School of Nursing, Chinese University of Hong Kong

Hong Kong

About this study

This study employed a quasi-experimental pretest-posttest design to compare online psychoeducation with conventional face-to-face psychoeducation. This study also included a qualitative study as process evaluation to explore the participants' experiences with the online psychoeducation.

Caregivers of people with dementia were recruited from two sources: elderly community centers and Facebook. Printed flyers were physically displayed in the elderly community centers and advertisements were posted on Facebook. Interested participants approached the principal investigator through telephone and were screened for eligibility. Informed consent was collected physically at the elderly community centers or via Google Forms.

The feasibility study required 30 participants per arm to test the intervention before a future definitive trial. Therefore, with two groups in this study, the total sample size was set at 60.

Participants recruited from the elderly community centers were allocated to the face-to-face group, whilst participants recruited from Facebook were allocated to the online group. The rationale for having a non-randomized design was to prevent potential contamination occurring due to information sharing among the participants. Participants were informed of the group allocation at the time of recruitment.

The sociodemographic data and outcomes were collected by an research assistant. All participants were also asked to complete the satisfaction questionnaire at T1. Questions for the satisfaction questionnaire and caregiving self-efficacy questionnaire were read out to participants.

Quantitative data were analyzed using the IBM SPSS Statistics version 26.0. Descriptive statistics were used to summarize the demographic data and the feasibility outcomes including recruitment rate, attrition rates, completion rate of intervention, participants' satisfaction score and completion rate of instrument. Chi-square test for the categorical variables and independent T-test for the continuous variables were used to examine the homogeneity of the participants in the two intervention groups. Analysis of Covariance was performed to examine between group differences in Revised Scale of Caregiving Self-Efficacy (RSCSE) score, with the respective pretest score as covariate. Paired T-test was also performed to examine within group differences in RSCSE score. Effect size was measured by dividing the mean difference within the group by the pooled standard deviation and reported as Cohen's d value. The cut-off points of small, medium and large effect size were 0.2, 0.5 and 0.8 respectively. All analysis was considered significant at p≤ 0.05 (2-tailed).

The audio-recorded interviews were transcribed verbatim for qualitative content analysis. The transcripts were managed with the support of Nvivo 14 for systematic organization of the data. The authors read the transcripts multiple times to get familiar with the data. They then coded the data and developed initial themes independently. Critical discussion and revision on the themes and subthemes were carried out until a consensus was reached. The main themes and subthemes were refined and named collaboratively. Illustrative quotes were selected through critical discussion between authors. The first author translated the quotes to English while the other authors helped with verification and proofreading.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • cognitively competent (i.e. Mini Mental State Examination ≥23)
  • taking care of a family member diagnosed with dementia of mild to moderate stage and required assistance in physical activities of daily living (ADL) (i.e. score ≥2 on the ADL scale
  • at least 5 hours of caregiving per week in the past month
  • had low caregiving self-efficacy (i.e. score ≤3 on the Caregiving Competence Scale

Exclusion criteria

  • currently participating in any other psychosocial interventional program
  • had psychiatric illnesses and had active treatment
  • did not had access to the Internet on any type of electronic device such as smart phone or laptop.

Treatment and study plan

online psychoeducation

Behavioral

Online psychoeducation aimed to enhance the knowledge and skill of family caregivers of people with dementia, who could not physically attend in-person class. Knowledge covering dementia caregiving including disease nature, communication skill, stress and coping, daily care, management of behavioral and psychological symptoms of dementia, and future planning. The intervention provided opportunities to practice through simulation and weekly home assignment. There was a total of 6 sessions and provided weekly. Each session lasted for 2 hours. Participants had discussion with peers and coached by a facilitator. Online psychoeducation wad delivered via Zoom videoconferencing.

Face-to-face psychoeducation

Behavioral

Face-to-face psychoeducation has the same content and flow of presentation as online psychoeducation.

Primary outcomes

  1. Sociodemographic background

    Time frame: Baseline

    Caregiver: Age, gender, marital status, relationship with care recipient, caregiving experience, education level, level of confidence in caregiving; Care recipient: age, gender, duration of dementia since diagnose, level of assistance required in activity daily living, stage of dementia

  2. Recruitment rate

    Time frame: Through study completion, an average of 6 months

    The proportion of eligible subjects and consented to join the study.

  3. Attrition rate

    Time frame: Through study completion, an average of 6 months

    The proportion of consented subjects who dropped out of the study. The reasons for attrition such as refusal were recorded.

  4. Completion rate

    Time frame: Through study completion, an average of 6 months

    The proportion of participants who attended at least 4 out of 6 sessions.

  5. Class attendance

    Time frame: Through study completion, an average of 6 months

    The proportion of participants who attended the class in each session

  6. Completion rate of study instrument

    Time frame: Through study completion, an average of 6 months

    The proportion of participants who completed the study instrument

  7. Satisfaction of intervention

    Time frame: On completion of intervention at 6 weeks

    Participants rated on the content, format and appropriateness of intervention on a 5-point Likert scale. The higher total score represented greater satisfaction with the intervention

  8. Experience of online psychoeducation

    Time frame: On completion of intervention at 6 weeks

    Individual semi-structured interviews were conducted to explore the experience of online psychoeducation.

Secondary outcomes

  1. Caregiving self-efficacy

    Time frame: Baseline and on completion of intervention at 6 weeks

    Participants completed the Revised Scale of Caregiving Self-efficacy. There are 15 questions in total and participant rated on a scale of 0-100 on each question. The mean score of 15 questions will be presented and the higher the score represented the higher level of caregiving self-efficacy.

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Official study title

An Evidence-based Online Psychoeducation for Family Caregivers of People With Dementia: A Feasibility Study

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 18, 2023
Registry last updated
Sep 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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