Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05892965

Instant Message-delivered Brief Internet-based Cognitive Behavioural Therapy (iCBT) for Post-stroke Depression: a Mixed Method Study

Led by The University of Hong Kong · Updated on 2024-07-11

160

Participants Needed

7

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of a therapist-guided, brief internet-based cognitive behavioural therapy (iCBT) delivered through instant messaging apps like WhatsApp and WeChat for people who have depression following a stroke. Post-stroke depression (PSD) is common and linked to worse health outcomes, but it is often not addressed adequately. This study aims to see if this personalized and synchronous messaging intervention can support stroke survivors with mild to moderate depressive symptoms and to understand their experience and adherence to the treatment. Participants will be randomly assigned to either the intervention group or the control group. The intervention group will receive a 3-month program of brief iCBT delivered via instant messages at their chosen times and frequencies, along with therapist-led text or voice messages providing real-time counselling and practical advice. The control group will receive general mental health information and reminders to complete follow-up surveys through instant messaging. The study will include 160 community-dwelling stroke survivors and will follow up at 6 months. During the study, researchers will assess depressive symptoms using the Patient Health Questionnaire-9 (PHQ-9) as the primary outcome at 24 weeks. They will also measure anxiety, stress, loneliness, and quality of life. Participants' experiences and compliance with the therapy will be explored in a post-trial qualitative study. The study uses strict methods following the CONSORT-EHEALTH guidelines and is led by The University of Hong Kong.

CONDITIONS

Brief Title

Instant Message-delivered Brief Internet-based Cognitive Behavioural Therapy (iCBT) for Post-stroke Depression

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of stroke (ICD-10 codes: I60-I69)
  • Age 18 years or older
  • Able to read and communicate in Chinese (Cantonese or Putonghua)
  • Able to use text or voice messaging on a smartphone
  • Cognitive screen (MoCA 5-minute Protocol) score of 14 or higher
  • Living in the community
  • Stroke occurred less than 1 year ago
  • Patient Health Questionnaire-9 (PHQ-9) score between 5 and 19 indicating mild to moderate depressive symptoms
Not Eligible

You will not qualify if you...

  • Diagnosis of psychiatric disease before stroke or currently taking psychotropic drugs including antidepressants
  • Severe depressive symptoms with PHQ-9 score 20 or higher
  • Currently participating in any psychological intervention

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 24 weeks

Participants receive brief internet-based cognitive behavioural therapy (iCBT) delivered via instant message, personalized to their preferences for message content, frequency, and timing, or receive general mental health information through instant message.

Regular instant message interactions throughout the period

Trial Site Locations

Total: 7 locations

1

Hong Kong PHAB Association

Hong Kong, Hong Kong

Actively Recruiting

2

Hong Kong Stroke Association

Hong Kong, Hong Kong

Actively Recruiting

3

NT West Community Rehabilitation Day Centre

Hong Kong, Hong Kong

Not Yet Recruiting

4

Queen Mary Hospital

Hong Kong, Hong Kong

Actively Recruiting

5

The Hong Kong Society for Rehabilitation

Hong Kong, Hong Kong

Actively Recruiting

6

Tung Wah Hospital

Hong Kong, Hong Kong

Actively Recruiting

7

United Christian Hospital

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

J

Jung Jae LEE

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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