Insomnia Clinical Trial
Official title:
Efficacy of Tai Chi Training to Alleviate Insomnia in Older Adults: A Randomized Controlled Trial
Verified date | July 2020 |
Source | The Hong Kong Polytechnic University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Elderly insomnia is a serious public health problem. Current conventional approaches for treating insomnia are not suitable or effective in elderly population. It has been previously demonstrated that Tai Chi has definite advantages to be developed as self-help therapy in older adults and has been preliminarily demonstrated to improve sleep in older people. This project aims to evaluate the efficacy of Tai Chi training on alleviating chronic insomnia in older adults.
Status | Completed |
Enrollment | 320 |
Est. completion date | August 2018 |
Est. primary completion date | February 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years and older |
Eligibility |
Inclusion Criteria: - 60 years or older - ethnic Chinese - fulfill the DSM-V criteria for chronic insomnia including difficulties to initiate sleep, maintain sleep or non-restorative sleep with complaint of impairment of daytime functioning, sleep difficulty occurs at least 3 nights per week and is present for at least three months. Exclusion Criteria: - cannot walk without assistive tool (e.g., cane) - any serious somatic condition that prevent participation for Tai Chi/generic fitness activities - current regular practicing of moderate exercise training or Tai Chi (>3 times a week of >30-min per session) - any serious chronic diseases known to affect sleep (e.g., cancer and autoimmune diseases) - under treatment of serious diseases known to affect sleep (e.g., cancer chemotherapy) - any chronic pain disorders known to affect sleep. |
Country | Name | City | State |
---|---|---|---|
China | The Chinese University of Hong Kong | Hong Kong | Hong Kong |
China | The Hong Kong Polytechnic University | Hong Kong | |
China | The University of Hong Kong | Hong Kong | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
Angus Yu | Chinese University of Hong Kong, Food and Health Bureau, Hong Kong, The University of Hong Kong |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Actigraphy-measured sleep onset latency | Objectively measured sleep onset latency (min) | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured sleep efficiency | Objectively measured sleep efficiency (%) | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured wake time after sleep onset | Objectively measured wake time after sleep onset (min) | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured total sleep time | Objectively measured total sleep time (min) | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured number of awakening | Objectively measured number of awakening (number of times) after sleep onset | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured average wake time | Objectively measured average wake time (min) of all awaken time after sleep onset | Immediately after completion of the 12 weeks intervention | |
Primary | Actigraphy-measured sleep onset latency | Objectively measured sleep onset latency (min) | 24 months after the completion of intervention | |
Primary | Actigraphy-measured Sleep efficiency | Objectively measured sleep efficiency (%) | 24 months after the completion of intervention | |
Primary | Actigraphy-measured wake time after sleep onset | Objectively measured wake time after sleep onset (min) | 24 months after the completion of intervention | |
Primary | Actigraphy-measured total sleep time | Objectively measured total sleep time (min) | 24 months after the completion of intervention | |
Primary | Actigraphy-measured number of awakening | Objectively measured number of awakening (number of times) after sleep onset | 24 months after the completion of intervention | |
Primary | Actigraphy-measured average wake time | Objectively measured average wake time (min) of all awaken time after sleep onset | 24 months after the completion of intervention | |
Secondary | Score of Pittsburgh Sleep Quality Index | Pittsburgh Sleep Quality Index is a questionnaire that assess sleeping quality with scale ranged from 0 to 21. (A smaller score suggests a better sleep quality) | Immediately after completion of the 12 weeks intervention and 24 months after the completion of intervention | |
Secondary | Change in dose of Sleep Medication | The change in dose of sleep medication used by the subjects after intervention. | Immediately after completion of the 12 weeks intervention and 24 months after the completion of intervention | |
Secondary | Score of Insomnia Severity Index | Insomnia Severity Index is a questionnaire that assess sleeping quality with scale ranged from 0 to 28. (A smaller score suggests a better sleep quality) | Immediately after completion of the 12 weeks intervention and 24 months after the completion of intervention | |
Secondary | 7-day Sleep Diary | Self-recorded sleep parameters (sleep onset latency, sleep efficiency, total sleep time, wake time after sleep onset, number of awakening and average awaken time) | Immediately after completion of the 12 weeks intervention and 24 months after the completion of intervention | |
Secondary | Treatment response rate | The percentage of participants that have their Score of Pittsburgh Sleep Quality Index reduced by at least 5 points | Immediately after completion of the 12 weeks intervention and 24 months after the completion of intervention | |
Secondary | Remission rate of insomnia | The percentage of participants that reached to remission of chronic insomnia according to DSM-5Immediately after the completion of the 12-week intervention | Immediately after completion of the 12-week intervention and 24-month after the complete completion of the 12-week intervention |
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