ClinicalTrials.Veeva

Menu

An Internet-based Self-help Intervention to Improve Common Mental Health Problems Among Medical Professionals (EMPOWER)

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Enrolling

Conditions

Depression, Anxiety

Treatments

Behavioral: E-training for Medical Professionals On Wellbeing and Effective Resolutions (E.M.P.O.W.E.R.)
Other: Education Materials

Study type

Interventional

Funder types

Other

Identifiers

NCT06910748
1007627352

Details and patient eligibility

About

This randomized controlled trial (RCT) aims to evaluate the effectiveness of an internet-based guided self-help intervention developed based on Problem Solving Therapy, a transdiagnostic low-intensity intervention recommended by the World Health Organization, in improving medical professionals' mental health.

Full description

Despite the high prevalence of common mental health problems among medical professionals (MPs), their help-seeking for mental health support is low due to barriers such as lack of time, shortage of mental health professionals, and the belief that mental health is not the priority. Existing interventions are empirically effective but practically challenging to be applied in Hong Kong given the long intervention hours and fixed schedule. New interventions are needed to cater for the unique needs of local MPs.

Objectives: An internet-based guided self-help intervention for MPs, E-training for Medical Professionals On Wellbeing and Effective Resolutions (the EMPOWER program), will be developed based on Problem Solving Therapy (PST), a transdiagnostic low-intensity intervention recommended by the World Health Organization. Targeted at local MPs aged 18-60 with depression and/or anxiety symptoms, the intervention aims to reduce their symptoms through strengthening coping skills for work-related problems. A randomized controlled trial (RCT) will be conducted to evaluate (1) the intervention's efficacy in reducing depression/anxiety compared with wait-list control (WLC); (2) its efficacy in improving the levels of PTSD, well-being, burnout, and work performance versus WLC; (3) the potential mediators/mechanisms explaining any between-group differences.

Method: 120 participants will be recruited online. The EMPOWER group will receive four 30-min self-paced weekly intervention sessions. The WLC will receive the intervention after the study period. Data will be collected at baseline, immediately post-intervention and 1-month follow-up. The group effect will be examined by comparing the mean improvement scores and remission rates on the outcome variables among the two groups. The potential mediation effects of adaptive problem solving strategies between the two groups and the outcomes will also be tested.

Expected outcomes: The investigators expect (1) greater reductions in depression and/or anxiety as well as levels of PTSD, well-being, burnout, and work performance for the EMPOWER group at post-treatment and 1-month follow-up than WLC, and that (2) the EMPOWER program will reduce depression and/or anxiety through enhancement in adaptive problem-solving strategies.

Implications: Findings can help to identify a cost-effective, flexible, and readily accessible mental health intervention for local MPs.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • (1) being a frontline doctor or nurse working in local public settings;
  • (2) at least 18 years of age;
  • (3) able to read and understand Chinese;
  • (4) have access to the Internet; and
  • (5) Patient Health Questionnaire (PHQ-9) and/or Generalized Anxiety Disorder (GAD-7) score>=5, indicating at least mild levels of depression and/or anxiety.

Exclusion criteria

  • (1) currently taking psychotropic medication; and
  • (2) actively suicidal.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

120 participants in 2 patient groups

The EMPOWER program
Experimental group
Description:
The intervention group will receive 4 weekly sessions (the EMPOWER program) in addition to the information about mental health, depression, anxiety and available treatment and community resources received by the waitlist control group.
Treatment:
Behavioral: E-training for Medical Professionals On Wellbeing and Effective Resolutions (E.M.P.O.W.E.R.)
Education materials
Active Comparator group
Description:
The waitlist control group receive education materials about mental health, depression, anxiety and available treatment and community resources but not the EMPOWER prgoram during the intervention period.
Treatment:
Other: Education Materials

Trial contacts and locations

1

Loading...

Central trial contact

Xue Yang, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems