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Clinical Trials/NCT04388800
NCT04388800CompletedNot Applicable

Development of an Online Cognitive Behavioral Intervention Program to Reduce Depressive Symptoms for Hong Kong People With Depression

Hong Kong Baptist University1 site in 1 country402 target enrollmentStarted: January 1, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
402
Locations
1
Primary Endpoint
Beck Depression Inventory-II (BDI-II)

Study Overview

Brief Summary

The purpose of this study is to develop a culturally and linguistically appropriate online cognitive behavioral intervention program-- with therapist guidance -- for Hong Kong Chinese adults suffering from major depressive disorder with mild to moderate depressive symptoms, and examine the effectiveness of this program in reducing their depressive symptoms and improving their mental health. The 3- and 6-month maintenance effect after 3 months and 6 months will also be tested.

Detailed Description

Previous studies have demonstrated that online cognitive behavioral therapy can significantly reduce depressive symptoms and improve mental health for people with depression. This project will develop an online cognitive behavioral intervention program (including both an online platform and a smartphone application) for Hong Kong people with depression. Blended mode will be delivered service, which include 8-week online program, 2 face-to-face sessions and 2 telephone follow-ups by a clinical psychologist. The program will be evaluated in its effectiveness in reducing depressive and anxiety symptoms, psychological distress, negative thoughts and negative emotions and increasing positive thoughts and positive emotions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Hong Kong resident
  • Has mild to moderate depressive symptoms
  • No suicidal risk in the past 3 months
  • Receive no face-to-face counselling since program commencement
  • Has access to a computer/smartphone with internet access
  • Has a valid email address
  • Exclusion criteria:
  • Has severe or no depressive symptoms
  • Has suicidal risk in the past 3 months
  • Currently receiving other psychological treatment
  • Suffer from severe psychiatric conditions, such as bipolar disorder or schizophrenia
  • Has no computer or smartphone with internet access
  • Has no valid email address

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Beck Depression Inventory-II (BDI-II)

Time Frame: 6 months

21-item rating scale for depressive symptoms

Patient Health Questionnaire-9 (PHQ-9)

Time Frame: 6 months

9-item rating scale for depressive symptoms.

Secondary Outcomes

  • General Health Questionnaire-12 (GHQ-12)(6 months)
  • Chinese Affect Scale (CAS)(6 months)
  • Beck Anxiety Inventory (BAI)(6 months)
  • Chinese Automatic Thoughts Questionnaire (CATQ)(6 months)
  • Negative effects Questionnaire (NEQ) (administered at post-test only)(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jiayan Pan

Associate Professor

Hong Kong Baptist University

Study Sites (1)

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