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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02260843
Other study ID # TaiChi and Insonmia
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2014
Est. completion date August 2018

Study information

Verified date July 2020
Source The Hong Kong Polytechnic University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Elderly insomnia is a serious public health problem. It has been estimated over 50% of elderly have sustained sleep complaints. About 20-40% of the elderly worldwide are reported insomniac. In Hong Kong, a high proportion (38%) of older people have been reported to have sleep disorders. These figures are alarming because insomnia associates with co-morbidities including cognitive impairment, depression, mood/anxiety disorders, risks for falls, hypertension, and heart disease in elderly. It also destructively affects daily functioning by impairing the memory and reducing the attention span and response time. Most importantly, insomnia has been evidently shown to link with the increased risk of hospitalization and mortality. As the proportion of geriatric population is rapidly increasing, it is foreseeable that the socioeconomic impact of elderly insomnia to the healthcare system will be undoubtedly aggravated.

Current conventional approaches for treating insomnia are not suitable or effective in elderly population. Pharmacologic treatment has always been a concern in insomniac senior patients due to the adverse drug effects including dependence, abuse, cognitive impairment and increase in risk of falls and hip fractures. With fewer adverse effects and consistent efficacy, cognitive behavioral therapy (CBT) is taken as a more appropriate remedy for elderly insomnia. However, the operation of effective CBT for insomnia is very labor demanding and cost-ineffective. The large-scale use of CBT for elderly insomnia is not feasible due to the shortage of CBT specialty-trained healthcare providers and the high treatment cost. The limited availability of CBT treatment is far insufficient to match with the increasingly large demand of insomniac elderly. There is another problem with the conventional approaches. It is observed that most of the insomnia sufferers would not seek timely clinical consultation and they tend to initiate self-help treatments when facing the problem of insomnia. This situation is suggested to be more common in Chinese elderly due to the traditional Confucius philosophy of reservation and quietness probably drive them more likely to keep the problem to themselves and become reluctant to seek prompt clinical help until serious medical symptom occurs. Given the prevalence of elderly insomnia is already high and keeps increasing, there is an urgent need to explore other effective therapeutic modalities preferably in forms of self-help remedies that can help to relieve the problem of elderly insomnia.

Tai Chi has definite advantages to be developed as self-help therapy in older adults. Tai Chi, a traditional form of Chinese fitness exercise, is a unique form of physical activity of low impact and slow body movement, which includes a meditation component. It is a moderate type of exercise that is well perceived to be suitable for regular practice by older population. It is expected that Tai Chi is more acceptable to the elderly patients to be incorporated with their daily life as an instant approach for remedying insomnia relative to the conventional clinical treatment such as CBT. Additional advantages of Tai Chi include low-cost and can be conveniently practiced at any time and any place without requirement for extensive facilities. Certainly, the practice of Tai Chi is more accessible than the conventional CBT treatment, which facilitates the large-scale use of Tai Chi to relieve insomnia in elderly population. Furthermore, Tai Chi can be practiced individually or in a group. If practicing in a group, Tai Chi provides additional benefit by serving as a vehicle for establishing social interaction through which older people can establish friendship and gain supports from other seniors.

Tai Chi has a number of beneficial effects on geriatric health and fitness. These health benefits include improvements of aerobic fitness, energy metabolism, muscular strength and balance. In addition to the improvements of cardiorespiratory function, bone loss, posture stability and flexibility, Tai Chi exercise has also been shown to improve psychological well-being via relieving symptoms of anxiety and depression and reducing mood disturbances. All these physical and psychological advantages of Tai Chi cooperatively support its prescription to the senior population.

Tai Chi has been preliminarily demonstrated to improve sleep in older people. Favorable effects on sleep parameters have been reported in geriatric following 12 weeks to 6 months of Tai Chi training. The self-reported sleep quality is demonstrated to be improved by a 12-week of Tai Chi intervention in the senior residents in elderly home. Favorable effects of 12-week of Tai Chi training in patients with chronic heart failure are reported by showing the enhancement of sleep stability as assessed by sleep spectrogram. A longer period (6-month) of Tai Chi training has also been shown to improve the Pittsburgh Sleep Quality Index (PSQI)-indicated sleep quality in community-dwelling older adults. In older subjects with moderate sleep complaint or sleep-disturbance, 24/25-week of Tai Chi training is shown to improve the self-rated sleep quality, habitual sleep efficiency, sleep duration, and sleep disturbance.

All these preliminary data collectively indicate the beneficial effects of Tai Chi on improving sleep in geriatric population. Nonetheless, all these studies have a common design limitation, which is the lack of direct objective sleep measures. With the study limitation and research gaps, the present project is proposed to examine the therapeutic effects of Tai Chi on chronic insomnia in elderly by including objective sleep measures. The findings of this project are expected to have impact to unveil the efficacy of Tai Chi to alleviate elderly insomnia, which has been an epidemic healthcare problem that necessitates to be tackled promptly.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Generic Fitness
Subjects in this group will receive three fitness lessons in a week while each session last for 1 hour for 12 weeks
Tai Chi Intervention
Subjects in this group will receive three tai chi lessons in a week while each session last for 1 hour for 12 weeks

Locations

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

Sponsors (4)

Lead Sponsor Collaborator
Angus Yu Chinese University of Hong Kong, Food and Health Bureau, Hong Kong, The University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

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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