Ecological Momentary Intervention for Stroke Caregivers' Psychological Support

Sponsor
The University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT04936828
Collaborator
(none)
256
8
2
21.4
32
1.5

Study Details

Study Description

Brief Summary

The proposed trial aims to evaluate the effectiveness of internet-delivered cognitive behavioural therapy (iCBT) based ecological momentary intervention (EMI) for psychological well-being in stroke family caregivers.

Condition or Disease Intervention/Treatment Phase
  • Other: iCBT-based EMI
N/A

Detailed Description

Many stroke patients require long-term care in the community. In Hong Kong (HK), most stroke caregivers in the community are family members, and many require psychological support for caregiver stress. However, these caregivers have difficulties accessing existing centre-based services due to varying work and care responsibilities, and therefore require alternative support services to meet their unique needs and schedules. Evidence shows that internet-delivered cognitive behavioural therapy (iCBT) is effective in managing psychological distress including depressive symptoms, especially when guided by healthcare professionals. Ecological momentary intervention (EMI) is an innovative and cost-effective intervention 'framework' that utilises mobile messages to deliver personalised psychological interventions. The proposed trial aims to deliver iCBT-based EMI through instant messaging applications (e.g. WhatsApp) to provide personalised and real-time psychological support led by nurses. Screened stroke caregivers with Patient Health Questionnaire-9 (PHQ-9) scores ranging from 5 to 19 (mild to moderately severe depressive symptoms) will be recruited from community centres, rehabilitation centres and outpatient clinics in HK. They will then be individually randomised into the Intervention group (n=128) or Control group (n=128). The Intervention group will receive the iCBT-based EMI for 12 weeks, which includes instant messages sent at the times and frequencies of the participants' choosing, and chat-based psychological support led by nurses to enhance effects of iCBT through real-time counselling and practical advice. The control group will only receive instant messages on general mental health information and reminders to participate in follow-up surveys. The primary outcome is PHQ-9 scores at 24 weeks. Secondary outcomes will include anxiety, perceived stress, caregiver burden, caring experience, spiritual well-being and quality-of-daily-life. We will strictly follow the CONSORT-EHEALTH checklist. A post-trial qualitative study will be conducted to understand the participants' experience of and compliance with the EMI. The intervention will be highly applicable for all caregivers requiring psychological support and will be one step further in meeting the World Health Organization's recommendations in supporting caregivers in the context of global ageing populations.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
256 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Other
Official Title:
Ecological Momentary Intervention for Stroke Caregivers' Psychological Support: a Randomised Controlled Trial
Actual Study Start Date :
Sep 17, 2021
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Receive iCBT based EMI with message content, delivery frequency and timing personalised to participants' preferences.

Other: iCBT-based EMI
Consists of brief iCBT for psychological support (mandatory), stroke care education (optional), and nurse-led real-time chat-based support messages, delivered according to participants' preferences.

No Intervention: Control group

Receive general mental health information through instant message.

Outcome Measures

Primary Outcome Measures

  1. Depressive symptoms (Patient Health Questionnaire-9 [PHQ-9]) [24-week]

    A 9-item scale with score ranging from 0 to 27, higher scores indicate higher severity of depressive symptom

Secondary Outcome Measures

  1. Anxiety symptoms (Generalized Anxiety Disorder-7 [GAD-7]) [24-week]

    A 7-item scale with score ranging from 0 to 21, higher scores indicate higher severity of anxiety symptoms

  2. Stress level (Perceived Stress Scale [PSS-4]) [24-week]

    A 4-item scale with score ranging from 0 to 16, higher scores indicate higher severity of stress

  3. Caregiver's burden (Zarit Burden Interview [ZBI-4]) [24-week]

    A 4-item scale with score ranging from 0 to 16, higher scores indicate higher severity of caregiving burden

  4. Caring experience (Positive Aspects of Caregiving [PAC]) [24-week]

    An 11-item scale with score ranging from 0 to 44, higher scores indicate more positive appraisal of caregiving experience

  5. Spiritual well-being (Sub-scale of Spirituality Scale for Chinese Elders [SSCE]) [24-week]

    An 8-item scale with score ranging from 0 to 32, higher scores indicate better spiritual well-being

  6. Quality of life (EuroQol 5-dimension 5-level questionnaire [EQ-5D-5L]) [24-week]

    A 5-item scale with predicted values ranging from -.864 to 1, higher values indicate higher health-related quality of life

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Primary family caregiver of stroke patient (modified Barthel Index [mBI] <15; usually represent moderate disability)

  • Able to read and communicate in Chinese

  • Aged ≥18

  • Able to use mobile phone text messaging function

  • PHQ-9 ranged from 5 to 19

Exclusion Criteria:
  • Professional medical personnel and professional carer

  • Has provided care for <1 month prior to recruitment

  • Has diagnosis of psychiatric disease or is currently taking psychotropic drug

  • PHQ-9 ≥ 20 (i.e., severe depressive symptom)

  • Currently participating in any type of psychological intervention (e.g., CBT)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hong Kong PHAB Association Hong Kong Hong Kong
2 Hong Kong Stroke Association Hong Kong Hong Kong
3 NT West Community Rehabilitation Day Centre Hong Kong Hong Kong
4 Queen Mary Hospital Hong Kong Hong Kong
5 Southern District Elderly Community Centre Hong Kong Hong Kong
6 The Hong Kong Society for Rehabilitation Hong Kong Hong Kong
7 Tung Wah Hospital Hong Kong Hong Kong
8 United Christian Hospital Hong Kong Hong Kong

Sponsors and Collaborators

  • The University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT04936828
Other Study ID Numbers:
  • 17617620
First Posted:
Jun 23, 2021
Last Update Posted:
Jul 27, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2022