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Clinical Trials/NCT05313542
NCT05313542UnknownNot Applicable

Effect of Physical Activity in the Format of Self-defence Training for Depressive Symptoms - A Pilot Randomised Controlled Trial

Chinese University of Hong Kong1 site in 1 country40 target enrollmentStarted: September 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
40
Locations
1
Primary Endpoint
Change in the Patient Health Questionnaire (PHQ-9)

Study Overview

Brief Summary

Inadequate mental health care capacity is a long-standing issue in Hong Kong (Yang & Mak, 2020). For example, a recent study predicts an additional 12% service need for specialist psychiatric care (Ni et al., 2020). It would be helpful to develop interventions that would ease the high demand of the health care system. Physical activity has been shown to reduce depressive symptoms in a number of studies (Bellón et al., 2021; Josefsson et al., 2014; Kvam et al., 2018; Schuch et al., 2016). Its flexibility and low-cost nature make physical activity a good intervention option for depressed individuals to do it anytime and anywhere.

This study aims to investigate the effect of physical activity intervention in the format of self-defence training on depressive symptoms. Around 40 eligible participants with at least moderate level of depressive symptoms will be randomly assigned to the physical activity (PA) group and waitlist (WL) control group. The PA group will receive a 6-week home-based self-defence training programme consisting of 120 min video training (including daily practice time) per week. Self-report questionnaires will be collected at baseline, immediate post-intervention, and 4-week follow up assessments. The primary outcome measure will be the Patient Health Questionnaire-9 to evaluate depression severity. Secondary outcomes will include psychological health symptoms, sleep quality, lifestyle, and quality of life. This research will provide new perspectives on the application of physical activity in the form of self-defence training as an intervention for depressive individuals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18 to 65 years old
  • •Hong Kong Residents
  • •Patient Health Questionnaire (PHQ-9) score ≥ 10; and
  • •Willingness to provide informed consent and comply with the trial protocol.

Exclusion Criteria

  • •Patients with any cardiovascular diseases
  • •Receiving psychological treatment or medication for psychiatric disorders
  • •Participated in self defence training in the past 6 months

Arms & Interventions

Physical Activity Group (PA group)

Experimental

The PA group will receive a 6-week home-based self-defence training programme consisting of 120 min video training (including daily practice time) per week. Self-report questionnaires will be collected at baseline, immediate post-intervention, and 4-week follow up assessments.

Intervention: Physical Activity (Behavioral)

Waitlist Group (WL group)

Other

The waitlist group will receive access to the programme at the end of study.

Intervention: Physical Activity (Behavioral)

Outcomes

Primary Outcomes

Change in the Patient Health Questionnaire (PHQ-9)

Time Frame: Baseline, immediately post-intervention, 4-week follow-up

The PHQ-9, a 20-item questionnaire used for screening, diagnosing, monitoring and measuring the severity of depression, which scores each of the nine DSM-IV criteria as "0" (not at all) to "3" (nearly every day).

Secondary Outcomes

  • Change in the Short Form (Six-Dimension) Health Survey (SF-6D)(Baseline, immediately post-intervention, 4-week follow-up)
  • Change in the International Physical Activities Questionnaire - Chinese version (IPAQ-C)(Baseline, immediately post-intervention, 4-week follow-up)
  • Change in Treatment Adherence Survey (TAS)(Baseline, immediately post-intervention)
  • Change in Hospital Anxiety and Depression Scale (HADS-14)(Baseline, immediately post-intervention, 4-week follow-up)
  • Change in Credibility-Expectancy Questionnaire (CEQ)(Baseline, immediately post-intervention, 4-week follow-up)
  • Change in the Insomnia Severity Index (ISI)(Baseline, immediately post-intervention, 4-week follow-up)
  • Change in Multidimensional Fatigue Inventory (MFI-20)(Baseline, immediately post-intervention, 4-week follow-up)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Fiona YY Ho

Assistant Professor

Chinese University of Hong Kong

Study Sites (1)

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