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Telephone-coached Graphic Narrative Bibliotherapy for Dementia Caregivers

Telephone-coached Graphic Narrative Bibliotherapy for Informal Caregivers of People With Dementia

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06413849
Enrollment
128
Registered
2024-05-14
Start date
2024-12-01
Completion date
2026-12-31
Last updated
2025-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiving Appraisal, Dementia Caregiver, Depressive Symptoms

Brief summary

This study aims to assess the efficacy of telephone-coached graphic narrative bibliotherapy in improving dementia caregiver depressive symptoms compared with the booklet group.

Detailed description

This is a two-arm cluster randomized controlled trial using a repeated-measures design to examine the effects of telephone-coached graphic narrative bibliotherapy on 128 (64 per group) informal caregivers of people with dementia. Participants in the intervention group will receive eight weekly telephone-coached graphic narrative bibliotherapy sessions, plus two face-to-face booster sessions and two follow-up sessions. The control group will receive an education booklet and check-in calls. Caregiver depressive symptoms, stress and anxiety, caregiving appraisal, care-recipient neuropsychiatric symptoms, and quality of life will be measured to test the intervention's effects immediately after completion and at a 6-month follow-up.

Interventions

OTHERTelephone coached graphic narrative bibliotherapy

Eight weekly sessions of telephone coached graphic narrative bibliotherapy

OTHERControl group

Reading educational booklet

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* provide unpaid care to a person diagnosed with early to moderate stage dementia; * provide at least 14 hours of care a week for at least 3 months * aged 18 years or above * able to read * have depressive symptoms * use a message application

Exclusion criteria

* with an unstable physical or mental condition * with cognitive impairment * receiving medical, psychological, or psychiatric treatment for depression * have been included in another interventional study

Design outcomes

Primary

MeasureTime frameDescription
Changes in depressive symptomsPre-intervention, immediately post-intervention, 6 months post-interventionDepressive symptoms will be measured with the Chinese version of the Depression Anxiety Stress Scale-21. It is a 4-point Likert scale consisting of 21 items that measure levels ofdepression, anxiety, and stress in participants. The total score ranges from 0-63, with the depression subscale score ranges from 0-21. Higher scores indicategreater severity of mental health problems.

Secondary

MeasureTime frameDescription
Changes in caregiving appraisalPre-intervention, immediately post-intervention, 6 months post-interventionCaregiving appraisal will be assessed using the Caregiving Appraisal Scale. It is a 26-item Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). The score ranges from 26 to 130. Higher scores on this scale indicate more positive caregiving appraisal.
Changes in stress and anxietyPre-intervention, immediately post-intervention, 6 months post-interventionStress and anxiety will be measured with the stress and anxiety subscales of the Depression, anxiety and stress scale-21 (DASS-21). The total score of the full scale ranges from 0-63, with the anxiety and stress subscale score both range from 0-21.
Changes in patient neuropsychiatric symptomsPre-intervention, immediately post-intervention, 6 months post-interventionPatient neuropsychiatric symptoms: will be measured with the Neuropsychiatric Inventory (NPI). NPI evaluates 12 common neuropsychiatric disturbances in dementia. The presence of problematic behaviors in each domain is assessed by asking an informant a screening question followed by a series of yes/no questions. The frequency of a symptom is created from 1 (rarely) to 4 (very often), and severity is rated from 1 (mild) to 3 (severe).
Changes in quality of lifePre-intervention, immediately post-intervention, 6 months post-interventionQuality of life will be measured with the Brief Older People's Quality of Life Questionnaire (OPQOL-Brief). It is a 13-item, 5-point Likert scale to measure the quality of life for older adults. The total score ranges from 13 to 65, with higher scores indicating a better quality of life.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026