DepressionCANDONCT04388800
Online Cognitive Behavioral Intervention Program for Hong Kong People With Depression
A study testing Confront and Navigate Depression Online (CANDO) in people with Depression, run by Hong Kong Baptist University at 1 site in Hong Kong.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 to 70 yearsHealthy volunteers can take part
- Conditions the study is for
- Depression
- What is being tested?
- Confront and Navigate Depression Online (CANDO)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 402 participants
- Where
- 1 siteHong Kong
- Study dates
- 1 Jan 2019to 30 Jun 2022
- Phase
- Interventional
- 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 to 70 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Development of an Online Cognitive Behavioral Intervention Program to Reduce Depressive Symptoms for Hong Kong People With Depression
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.
Read the 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.
- Conditions
- Depression
- Being tested
- Confront and Navigate Depression Online (CANDO)
- Keywords
- online cognitive behavioral intervention, Hong Kong Chinese, depression
- Medical subject headings
- Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Confront and Navigate Depression Online (CANDO)Other
This study adopts a blended mode of service delivery, which included both online and offline intervention. The online intervention includes 8 weekly online model, animation briefing and debriefing, case demonstration video, exercise, forum, internal messaging, reminder, online assessment, session review and online booking system. The offline intervention includes two face-to-face sessions and two telephone follow-ups.
| Study group | Role | What they receive |
|---|---|---|
| web-based cognitive behavioral intervention | Experimental | The web-based program is consisted of 8 online modules, forum, internal messaging, reminder, online assessment and online booking. Each online module contains mood check, animation briefing and debriefing, case demonstration videos, session review and exercise.
Blended mode is adopted to deliver service, which includes the online program, two face-to-face session and 2 telephone follow-ups with a clinical psychologist. Receives: Other: Confront and Navigate Depression Online (CANDO) |
| app-based cognitive behavioral intervention | Experimental | App-based cognitive behavioral intervention program The App-based program is consisted of 8 online modules, forum, internal messaging, reminder, online assessment and online booking. Each online module contains mood check, animation briefing and debriefing, case demonstration videos, session review and exercise.
Blended mode is adopted to deliver service, which includes the online program, two face-to-face session and 2 telephone follow-ups with a clinical psychologist Receives: Other: Confront and Navigate Depression Online (CANDO) |
| Wait-list control group | No intervention | No intervention will be provided when the experimental group is receiving services, but the access to the app-based program will be delivered to the wait-list control group after the two experimental groups complete the service. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Beck Depression Inventory-II (BDI-II)
21-item rating scale for depressive symptoms
Measured: 6 months
Patient Health Questionnaire-9 (PHQ-9)
9-item rating scale for depressive symptoms.
Measured: 6 months
Secondary outcomes (5)
General Health Questionnaire-12 (GHQ-12)
12 item rating scale for psychological distress.
Measured: 6 months
Beck Anxiety Inventory (BAI)
21-item rating scale for symptoms of anxiety.
Measured: 6 months
Chinese Automatic Thoughts Questionnaire (CATQ)
20-item rating scale for automatic thoughts.
Measured: 6 months
Chinese Affect Scale (CAS)
20-item rating scale for positive and negative emotions of Chinese-speaking people.
Measured: 6 months
Negative effects Questionnaire (NEQ) (administered at post-test only)
20-item rating scale for negative effects caused by psychological treatment
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 May 2020
- Study start1 Jan 2019
- Primary completion30 Jun 2022
- Study completion30 Jun 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for DepressionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- randomized controlled trial
- Masking
- None (open label)
- Enrolment
- 402 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hong Kong Baptist University
- Sponsor type
- University, hospital or other
- Collaborators
- Stockholm University, Richmond Fellowship of Hong Kong, Caritas Wellness Link - Tsuen Wan, Dr. Chiu Siu Ning, Innovation and Technology Fund for Better Living
- Responsible party
- Principal investigator, Jiayan Pan, Hong Kong Baptist University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04388800
- Sponsor's protocol ID
- ITB/FBL/5002/18/P
- Acronym
- CANDO
- Status last verified
- Sep 2023
- First submitted
- 12 May 2020
- Last updated
- 22 Sep 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Pan JY, Rafi J. Culturally Adapted Guided Internet-Based Cognitive Behavioral Therapy for Hong Kong People With Depressive Symptoms: Randomized Controlled Trial. J Med Internet Res. 2025 Feb 25;27:e64303. doi: 10.2196/64303.
PubMed 39998865
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development of an Online Cognitive Behavioral Intervention Program to Reduce Depressive Symptoms for Hong Kong People With Depression
- ClinicalTrials.gov ID
- NCT04388800
- Acronym / sponsor ID
- CANDO / ITB/FBL/5002/18/P
- Conditions
- Depression
- Keywords
- online cognitive behavioral intervention, Hong Kong Chinese, depression
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 402 participants (actual)
- Lead sponsor
- Hong Kong Baptist UniversityUniversity, hospital or other
- Collaborators
- Stockholm University, Richmond Fellowship of Hong Kong, Caritas Wellness Link - Tsuen Wan, Dr. Chiu Siu Ning, Innovation and Technology Fund for Better Living
- Study start
- 1 Jan 2019 (actual)
- Primary completion
- 30 Jun 2022 (actual)
- Study completion
- 30 Jun 2022 (actual)
- First posted
- 14 May 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| web-based cognitive behavioral intervention | Experimental | Other: Confront and Navigate Depression Online (CANDO)The web-based program is consisted of 8 online modules, forum, internal messaging, reminder, online assessment and online booking. Each online module contains mood check, animation briefing and debriefing, case demonstration videos, session review and exercise. Blended mode is adopted to deliver service, which includes the online program, two face-to-face session and 2 telephone follow-ups with a clinical psychologist. |
| app-based cognitive behavioral intervention | Experimental | Other: Confront and Navigate Depression Online (CANDO)App-based cognitive behavioral intervention program The App-based program is consisted of 8 online modules, forum, internal messaging, reminder, online assessment and online booking. Each online module contains mood check, animation briefing and debriefing, case demonstration videos, session review and exercise. Blended mode is adopted to deliver service, which includes the online program, two face-to-face session and 2 telephone follow-ups with a clinical psychologist |
| Wait-list control group | No intervention | –No intervention will be provided when the experimental group is receiving services, but the access to the app-based program will be delivered to the wait-list control group after the two experimental groups complete the service. |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (6 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Confront and Navigate Depression Online (CANDO)This study adopts a blended mode of service delivery, which included both online and offline intervention. The online intervention includes 8 weekly online model, animation briefing and debriefing, case demonstration video, exercise, forum, internal messaging, reminder, online assessment, session review and online booking system. The offline intervention includes two face-to-face sessions and two telephone follow-ups. | Other | app-based cognitive behavioral intervention, web-based cognitive behavioral intervention |
Primary outcome
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.
5 secondary outcomes
General Health Questionnaire-12 (GHQ-12)
Time frame: 6 months
Beck Anxiety Inventory (BAI)
Time frame: 6 months
Chinese Automatic Thoughts Questionnaire (CATQ)
Time frame: 6 months
Chinese Affect Scale (CAS)
Time frame: 6 months
Negative effects Questionnaire (NEQ) (administered at post-test only)
Time frame: 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2023.
- Derived from this study: PubMed 39998865Pan JY, Rafi J. Culturally Adapted Guided Internet-Based Cognitive Behavioral Therapy for Hong Kong People With Depressive Symptoms: Randomized Controlled Trial. J Med Internet Res. 2025 Feb 25;27:e64303. doi: 10.2196/64303.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Confront and Navigate Depression Online (CANDO) in people with Depression, run by Hong Kong Baptist University 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 6 inclusion and 6 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 22 Sep 2023. 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?
Beck Depression Inventory-II (BDI-II) (time frame: 6 months). 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 NCT04388800, which also lists 1 linked publication.
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 22 Sep 2023.