Important Note: Redirection of Services to ChiCTR
We would like to inform you that the Clinical Trial Registry page will discontinue the function of updating trial information directly on this platform. However, you will still be able to view the existing registration details. For any updates to trial information, you can use the China Clinical Trial Registry (ChiCTR) directly at https://www.chictr.org.cn. This change will be fully implemented by 2024-Aug-05. Thank you for your attention.
CUHK_CCT00438
2014-11-10
Prospective
2014.473-T
Chen Wai Wai Vivien Foundation Ltd
Chen Wai Wai Vivien Foundation Therapeutic Physical Mental Exercise Centre, Department of Psychiatry, The Chinese University of Hong Kong
N/A
Ms Harriet W Y Tang 鄧穎瑜
Room 3A, Block E, Staff Quarters, Prince of Wales Hospital, 46 Ngan Shing Street, Shatin
852-28314305
harriet@cuhk.edu.hk
Department of Psychiatry, The Chinese University of Hong Kong
Prof. Linda CW Lam 林翠華
Department of Psychiatry, G/F Multi-Centre, Tai Po Hospital, Tai Po. NT, Hong Kong
852-26076027
cwlam@cuhk.edu.hk
Department of Psychiatry, the Chinese University of Hong Kong
Aerobic and mind body exercise interventions for adults with anxiety and depressive disorders under primary care settings in Hong Kong – a randomized control trial.
Aerobic and mind body exercise interventions for adults with anxiety and depressive disorders under primary care settings in Hong Kong – a randomized control trial.
個人化身心運動治療對抑鬱症及焦慮症之隨機對照臨床試驗效果研究
A study on the effects of mind body exercise on depression and anxiety
Hong Kong SAR, China
Yes
2014-10-22
Major Depressive Episode or Generalized Anxiety Disorder
Behavior
Aerobic and mind body exercise interventions
6 weeks intervention
6 week intervention of either mind body exercise intervention or educational health talk
1. Subject from 18 to 60 years old
2. Clinical Diagnosis of Major Depressive Episode or Generalized Anxiety Disorder
3. Currently undergoing treatment for the mood disorder in a priamry care setting
1. Other comorbid psychiatric diagnosis
2. Physically unfit to exercise as assessed by physiotherapist.
3. Pregnant
18
60
Both Male and Female
Interventional
Randomized
Placebo
Single-blind
Parallel
2014-11-22
80
Not Yet Recruiting
Primary outcome measure will be the Hospital Anxiety Depression Scale (HADS). Assesment and records of adverse events will be conducted at baseline, 6th week and 12th weeks.
Secondary outcomes include the Sheehan Disability Scale, Pittsburgh Sleep Quality Index, 12 item Short Form Health Survey and Fitbit Flex wristband monitor for mobilizaiton pattern. Assesment and records of adverse events will be conducted at baseline, 6th week and 12th weeks.
2015-12-10
Yes
N/A
|
|
|
|
|
---|---|---|---|---|
No documents yet. |