NCT05510453

Brief Summary

Studies have found up to 75% of mental disorders in adulthood have their onset before the age of 25 (Lin et al., 2008; Kessler et al., 2005), suggesting youth marks a critical period of intervention. Across the various psychiatric conditions, depressive and anxiety disorders have consistently been reported to be two of the most common conditions in young people globally (Merikangas et al., 2010; Racine et al., 2021). Both depressive and anxiety disorders are related to various negative impacts on youths' lives, such as undermining academic achievements, with other negative influences found in past studies (Birmaher et al., 1996; Fletcher, 2008, Woodward and Fergusson, 2001; Swan and Kendall, 2016). Notably, an increasing number of studies have found not only can clinical disorders, but also early symptoms of such conditions, can cause significant burden on the individual, their family and peers, as well as the larger society (Spencer et al., 2018; Lynch and Clarke, 2006; Wingrove and Rickwood, 2020). Existing healthcare services, however, tend to prioritise service targeting those with severe mental health needs. Knowledge about subtle mental health symptoms is lacking among the general public, which can contribute to delayed care and treatment (Fung et al., 2021). In addition, mental health services in Hong Kong are not only characterised by long waiting times but are also coupled with significant stigma, which can in turn prevent help-seeking, especially among young people (Sun et al., 2017; Yap, Wright, and Jorm, 2011). In view of the significance of early engagement and intervention for those with mental health needs and the current situation in Hong Kong, the implementation of low-intensity online-based interventions (LiON) for mental health appears to be a largely promising approach. Low-intensity refers to low usage of "specialist therapist time" (Bower and Gilbody, 2005), or usage in a cost-effective way, such as in a group-based Cognitive Behavioural Therapy context. Low-intensity interventions focus on delivering self-help and self-management skills which can be led by non-specialists, which in turn help to reduce the cost required in both training and the delivering of intervention. Recent studies have also increasingly highlighted young people's preference to access mental health services through online platforms (Becker et al., 2016). Due to limited mental health resources and the high demand for mental health services in Hong Kong, such online-based low-intensity interventions - when shown to be effective - can be largely helpful in reducing societal costs, reduce the barriers to help-seeking, and facilitate large-scale implementation of mental health services on a population level. This study will adopt an open labelled wait list RCT design. Participants will be randomly assigned using a computer-generated sequence into either the (i) low-intensity online intervention (LiON) group (n = 60) or (ii) wait list control (WLC) group (n = 60) in one-to-one ratio. This study design was adopted to ensure all participants will be able to receive LiON during the period of this study. Random blocks of the size of 4 will be used for randomisation. Stratification will also be applied according to their distress severity (as measured by the Kessler Psychological Distress Scale). Those randomised to the LiON intervention group will first receive the 4-week LiON, with generic self-help tips provided to each participant before completing the T2 assessment. Meanwhile, those randomised to the WLC group will first receive generic self-help tips for a period of 4 weeks, followed by the 4-week LiON before completing the T2 assessment. Prior to the commencement of the LiON, all participants will first be screened for eligibility for participation by a professional clinician of the research team (i.e., psychiatrists or psychologist, senior social worker). A review session via Zoom will also be first provided by the trained interventionist (who will be a graduate with background in psychology, social work, or other related mental health disciplines with prior and ongoing training from senior clinicians of the research team) to each participant to determine his or her needs and ensure all inclusion and exclusion criteria are met. Briefing about the LiON, such as module structure and components of focus will also be provided during this session. All participants will also be provided with generic self-help tips. For those in the LiON intervention group, these self-help tips will be provided after the 4-week LiON. For those in the WLC group, these self-help tips will be provided during the first 4 weeks after randomisation.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 18, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 22, 2022

Completed
10 days until next milestone

Study Start

First participant enrolled

September 1, 2022

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2024

Completed
Last Updated

August 25, 2022

Status Verified

August 1, 2022

Enrollment Period

1.3 years

First QC Date

August 18, 2022

Last Update Submit

August 22, 2022

Conditions

Outcome Measures

Primary Outcomes (3)

  • Symptoms of depression

    Depression subscale (DASS-D) of the 21-item Depression Anxiety Stress Scale (DASS). The scores range from 0 to 42. Higher scores indicate greater depressive symptoms

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Symptoms of anxiety

    Anxiety subscale (DASS-A) of the 21-item Depression Anxiety Stress Scale (DASS). The scores range from 0 to 42. Higher scores indicate greater anxiety symptoms.

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Symptoms of distress

    6 items from the Kessler Kessler Psychological Distress Scale (K6)

    Changes from baseline to immediate post-intervention to 1-month post-intervention

Secondary Outcomes (6)

  • Functioning - days of reduced productivity

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Functioning - days of complete productivity loss

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Perceived sleep quality

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Perceived stress level

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • Stress coping abilities

    Changes from baseline to immediate post-intervention to 1-month post-intervention

  • +1 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL
Other: Low-intensity online intervention (LiON)

Wait-list control

OTHER
Other: Low-intensity online intervention (LiON)

Interventions

The LiON in the current study is comprised of three core modules identified to be core areas of stress and needs of participants based on clinical experiences of the research team. The three modules include (1) stress management, (2) sleep and relaxation, and (3) problem-solving skills. Each module consists of four 1-on-1 sessions which will be conducted through online platforms (such as Zoom) that lasts for 45 minutes. Participants will attend these sessions once a week. The control group will receive the intervention after a waiting period of 4 weeks.

InterventionWait-list control

Eligibility Criteria

Age12 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • young people aged between 12-30
  • who have sufficient proficiency in Chinese to understand verbal and written instructions and give informed consent
  • with symptoms of mental distress (K6≥ 5).

You may not qualify if:

  • receiving any form of cognitive behavioural therapy (CBT)
  • active suicidal ideation/attempts within the past one month, serious suicidal ideation or self harm risks
  • inability to turn on camera for the course of the LiON intervention
  • inability to provide emergency contact
  • located outside of Hong Kong
  • history of organic brain disorder, psychosis, learning disability (e.g., special school attendance)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Hong Kong

Hong Kong, Hong Kong

Location

Related Publications (1)

  • Suen YN, Hui CLM, Lei LKS, Leung CM, Wong SMY, Lai GCH, Chau EHS, Wong MTH, Chan SKW, Wong GHY, Chen EYH. Low-Intensity Online Intervention for Mental Distress Among Help-Seeking Young People in Hong Kong: A Randomized Clinical Trial. JAMA Netw Open. 2025 Jan 2;8(1):e2454675. doi: 10.1001/jamanetworkopen.2024.54675.

Central Study Contacts

Yi Nam Suen

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant Professor

Study Record Dates

First Submitted

August 18, 2022

First Posted

August 22, 2022

Study Start

September 1, 2022

Primary Completion

December 31, 2023

Study Completion

June 30, 2024

Last Updated

August 25, 2022

Record last verified: 2022-08

Data Sharing

IPD Sharing
Will not share

Locations