Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
30 participants
INTERVENTIONAL
2018-11-01
2020-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Treatment Group
lifestyle medicine group
Lifestyle Medicine
Lifestyle intervention including diet, sleep, exercise, relaxation and mindfulness
CAU group
Care-As-Usual group
No interventions assigned to this group
Interventions
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Lifestyle Medicine
Lifestyle intervention including diet, sleep, exercise, relaxation and mindfulness
Eligibility Criteria
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Inclusion Criteria
2. Cantonese language fluency;
3. Patient Health Questionnaire (PHQ-9) score ≥ 10; and
4. Willingness to provide informed consent and comply with the trial protocol.
Exclusion Criteria
2. Have suicidal ideation based on Beck Depression inventory (BDI-II) Item 9 score ≥ 2 (referral information to professional services will be provided to those who endorsed items on suicidal ideation);
3. Using medication or psychotherapy for depression;
4. Having unsafe conditions and are not recommended for exercising or a change in diet by physicians; and
5. Have major psychiatric, medical or neurocognitive disorders that make participation infeasible or interfere with the adherence to the lifestyle modification.
18 Years
ALL
No
Sponsors
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The Hong Kong Polytechnic University
OTHER
The University of Hong Kong
OTHER
University of Western Sydney
OTHER
University of Melbourne
OTHER
Chinese University of Hong Kong
OTHER
Responsible Party
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Fiona YY Ho
Assistant Professor
Locations
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The Chinese University of Hong Kong
Hong Kong, , Hong Kong
Countries
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Facility Contacts
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Other Identifiers
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PSY003
Identifier Type: -
Identifier Source: org_study_id
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