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Common Mental Disorders (CMD)NCT07522775

Durability of the Effects of Low-Intensity Cognitive Behavioural Therapy

An observational study of Common Mental Disorders (CMD), run by New Life Psychiatric Rehabilitation Association at 1 site in Hong Kong.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This exploratory study investigates the relapse condition in Hong Kong adults after low-intensity cognitive behavioural therapy (LICBT) treatment for 18 to 48 months with a 6-month interval. Individuals who received LICBT treatment between 2017 and 2020 will be recruited to assess their current mental health status. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Common Mental Disorders (CMD)
What is being tested?
Low-intensity cognitive behavioural therapy
How many people
806 participants
Where
1 siteHong Kong
Study dates
2 Oct 2021to 9 Apr 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Participants were service users of a community mental health project in Hong Kong.

Who may be able to join

  • Aged 18 years old or above,
  • Capable of understanding Cantonese,
  • Received at least 2 sessions of LICBT since September 2017.

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Hong Kong1 site
  • New Life Psychiatric Rehabilitation Association

    Hong Kong

Other trials in Hong Kong

About this study

Official title: Durability of the Therapeutic Effects of Low-Intensity Cognitive Behavioural Therapy for Common Mental Disorders: a Long Term Follow-up on Relapse

This exploratory study investigates the relapse condition in Hong Kong adults after low-intensity cognitive behavioural therapy (LICBT) treatment for 18 to 48 months with a 6-month interval. Individuals who received LICBT treatment between 2017 and 2020 will be recruited to assess their current mental health status. It is hypothesised that the improvements in depression and anxiety scores will be maintained at 18-to-48-month follow-up.

Read the detailed description

The most prevalent common mental disorders worldwide are depression and anxiety. A local morbidity study illustrated that the prevalence rate for any common mental disorders is 13.3% in Hong Kong. Due to the huge demand for mental health services in Hong Kong, the waiting time for a new referral is around 1 year. Psychotherapies are suggested as first-line treatment for mood disorders, and while the effectiveness of traditional cognitive behavioural therapy (CBT) is consistently replicated, it is comparatively expensive and time-consuming. As a result, the delivery of traditional CBT alone cannot handle the huge demands for mental health service usage. To tackle this challenge, low-intensity cognitive behavioural therapy (LICBT) was developed in the United Kingdom (UK) to help individuals with lower severity of common mental disorders.

Local effectiveness of LICBT was supported by a pilot study in a Hong Kong community centre. In accordance with the UK National Institute for Health and Care Excellence (NICE) guidelines, service users were offered a brief treatment comprising six to eight structured sessions, in which they were assessed to identify the presenting problems and taught psychological tools to cope with their distress. Large effect sizes were reported for clinical improvements in depression and anxiety and satisfactory outcomes were also achieved. Despite the strong support for the short-term benefits of LICBT, depression and anxiety disorders are prone to relapse. Therefore, it is of great interest to investigate the long-term effects of LICBT.

Being tested
Low-intensity cognitive behavioural therapy
Keywords
LICBT, Follow-up

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Low-intensity cognitive behavioural therapyBehavioural

    Low-intensity cognitive behavioural therapy (LICBT) is a briefer form of the traditional cognitive behavioural therapy developed to help individuals with a lower severity of common mental disorders. LICBT is conducted in the form of individual guided self-help and comprises six to eight structured sessions in which psychological tools such as behavioural activation, worrying time, problem solving, exposure and habituation, and exposure and response prevention are taught.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Patient Health Questionnaire-9 (PHQ-9)

    The Patient Health Questionnaire-9 is a 9-item self-report questionnaire used to assess the severity of depressive symptoms. Total scores on the PHQ-9 range from 0 to 27. Scores of 5, 10, 15, and 20 represent mild, moderate, moderately severe, and severe depression, respectively.

    Measured: Follow-up at 18-48 months after treatment

  2. Generalized Anxiety Disorder-7 (GAD-7)

    The Generalized Anxiety Disorder-7 is a 7-item self-report questionnaire used to assess the severity of anxiety symptoms. Total scores on the GAD-7 range from 0 to 21. Scores of 5, 10, and 15 represent mild, moderate, and severe anxiety, respectively.

    Measured: Follow-up at 18-48 months after treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Apr 2026
  2. Study start2 Oct 2021
  3. Primary completion9 Apr 2022
  4. Study completion9 Apr 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
806 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07522775
Sponsor's protocol ID
CREC 2021.421
Status last verified
Apr 2026
First submitted
2 Apr 2026
Last updated
13 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Bruce SE, Yonkers KA, Otto MW, Eisen JL, Weisberg RB, Pagano M, Shea MT, Keller MB. Influence of psychiatric comorbidity on recovery and recurrence in generalized anxiety disorder, social phobia, and panic disorder: a 12-year prospective study. Am J Psychiatry. 2005 Jun;162(6):1179-87. doi: 10.1176/appi.ajp.162.6.1179.

    PubMed 15930067
  • Powell CLYM, Lo AP, Yeung GTY, Leung NTY, Mak WWS, So SHW, Chiu CD, Yau SSW, Mullan EG, Leung PWL. A pilot study on the effectiveness of low-intensity cognitive behavioural therapy (LiCBT) for common mental disorders in Hong Kong. Behav Cogn Psychother. 2021 Nov;49(6):758-763. doi: 10.1017/S1352465820000971. Epub 2021 Jan 13.

    PubMed 33436141
  • Lam LC, Wong CS, Wang MJ, Chan WC, Chen EY, Ng RM, Hung SF, Cheung EF, Sham PC, Chiu HF, Lam M, Chang WC, Lee EH, Chiang TP, Lau JT, van Os J, Lewis G, Bebbington P. Prevalence, psychosocial correlates and service utilization of depressive and anxiety disorders in Hong Kong: the Hong Kong Mental Morbidity Survey (HKMMS). Soc Psychiatry Psychiatr Epidemiol. 2015 Sep;50(9):1379-88. doi: 10.1007/s00127-015-1014-5. Epub 2015 Feb 8.

    PubMed 25660760
  • Clark DM. Realizing the Mass Public Benefit of Evidence-Based Psychological Therapies: The IAPT Program. Annu Rev Clin Psychol. 2018 May 7;14:159-183. doi: 10.1146/annurev-clinpsy-050817-084833. Epub 2018 Jan 19.

    PubMed 29350997
  • Burcusa SL, Iacono WG. Risk for recurrence in depression. Clin Psychol Rev. 2007 Dec;27(8):959-85. doi: 10.1016/j.cpr.2007.02.005. Epub 2007 Mar 3.

    PubMed 17448579

Questions about this trial

What is this clinical trial studying?

An observational study of Common Mental Disorders (CMD), run by New Life Psychiatric Rehabilitation Association at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patient Health Questionnaire-9 (PHQ-9) (time frame: Follow-up at 18-48 months after treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07522775, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.

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