ClinicalTrials.Veeva

Menu

E-bibliotherapy for Informal Caregivers of People With Dementia

T

The Hong Kong Polytechnic University

Status

Not yet enrolling

Conditions

Psychological Well-Being
Caregiver Stress Syndrome
Dementia

Treatments

Other: Control
Other: E-bibliotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05927805
HSEARS20221020009

Details and patient eligibility

About

The objective of this study is to test the efficacy of e-bibliotherapy on improving the psychological well-being of informal caregivers of people with dementia as compared with a control group.

Full description

This project is a two-arm randomized controlled trial evaluating the effects of e-bibliotherapy on improving the psychological well-being of informal caregivers of people with dementia. One hundred and ninety-two informal caregivers of people with dementia will be recruited. Participants in the intervention group will receive eight weekly e-bibliotherapy sessions. The control group will get access to the same e-bibliotherapy app but accept only general daily living knowledge. Psychological well-being, caregiving appraisal, mental health, biomarker of stress, and health-related quality of life will be measured to test the effects of e-bibliotherapy immediately post-intervention, three months post-intervention, and six months post-intervention. Focus group interviews will be conducted immediately post-intervention to explore caregivers' experiences participating in this study.

Enrollment

192 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • primary caregivers aged 18 or above;
  • provide unpaid regular care to a person with mild to moderately severe dementia (measured by Global Deterioration Scale, GDS=4~6);
  • have cared for the care recipient for at least six months;
  • assist with at least one of the care recipient's daily activities;
  • use a smartphone or tablet;
  • can read Chinese.

Exclusion criteria

  • caregivers with unstable physical or mental conditions;
  • have cognitive impairment;
  • are undergoing acute treatment or have not yet stabilized on their chronic medication;
  • are involved in another interventional study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

192 participants in 2 patient groups

Intervention group
Experimental group
Description:
Eight weekly sessions of e-bibliotherapy. Participants in the intervention group will use the e-bibliotherapy app we develop, and accept e-bibliotherapy via the app.
Treatment:
Other: E-bibliotherapy
Control group
Sham Comparator group
Description:
Eight weekly sessions of self-learning of general daily living knowledge that this different from the intervention contents from the same e-bibliotherapy app.
Treatment:
Other: Control

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems