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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05808517
Other study ID # V1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2022
Est. completion date December 31, 2022

Study information

Verified date March 2023
Source The Hong Kong Polytechnic University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators designed an RCT aimed at 1) exploring the effectiveness of combining TC with rTMS for synergistically improving sleep disturbances in community-dwelling older adults, 2) investigating the mediating roles of arousal states as the underlying mechanism of the potential beneficial effects, and 3) evaluating the feasibility and safety to inform the clinical practice. The investigators hypothesized that integrating TC and rTMS can affect the different dimensions of the arousal system to improve sleep disturbances with optimized clinical outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: 1. Classified with sleep disturbances (indications of poor sleep quality with a score >5 in Pittsburgh Sleep Quality Index) 2. Education level at primary or higher, and able to communicate in Cantonese (3) No experience of mind-body exercising such as TC, Qigong, or yoga within the past 6 months Exclusion Criteria: 1. Serious visual or hearing difficulty 2. Active suicidal ideation or self-harm behaviors 3. Cognitive impairment (a score <26 in the Montreal Cognitive Assessment) 4. Comorbid diagnoses such as mental disorders, organic brain syndrome, or intellectual disabilities 5. Cardiac pacemaker, implanted medication pump, the intracranial implant (e.g., aneurism clips, shunts, stimulators, cochlear implants, or electrodes), or any other metal object within or near the head 6. Receiving other treatments or participating in other clinical trials during the same period 7. Current severe medical condition preventing physical exercise

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Tai Chi
Tai Chi (TC) is a traditional Chinese exercise, also known as a mind-body exercise. It is suitable as an alternative or supplementary form of routine physical exercise for older adults. TC focuses on gentle and rhythmical movements while maintaining a meditative state. Low to moderate activities have benefits to improve sleep disturbances in older adults. In addition, growing evidence widely supports meditation as a potential intervention to improve sleep disturbances through reducing repetitive negative thoughts such as worry and rumination.
Other:
repetitive transcranial magnetic stimulation
The brain stimulation technique repetitive transcranial magnetic stimulation (rTMS) provides the opportunity to non-invasively modulate cortical excitability. In general, low-frequency rTMS (= 1 Hz) is thought to inhibit cortical excitability.

Locations

Country Name City State
Hong Kong The Hong Kong Polytechinic University Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary The change from baseline (T0) Insomnia Severity Index at immediately after the intervention (T1) and 3-month follow-up (T2) Baseline (T0), immediately after the intervention (T1), and 3-month follow-up (T2)
Secondary The change from baseline (T0) somatic and cognitive arousal assessed by Pre-Sleep Arousal Scale at immediately after the intervention (T1) and 3-month follow-up (T2) Baseline (T0), immediately after the intervention (T1), and 3-month follow-up (T2)
Secondary The change from baseline (T0) cortical arousal measured by 15 minutes eye-closed state electroencephalogram (EEG) at immediately after the intervention (T1) and 3-month follow-up (T2) Baseline (T0), immediately after the intervention (T1), and 3-month follow-up (T2)
Secondary The change from baseline (T0) sleep pattern assessed by an objective measurement (wrist ActiGraph GT3X) at immediately after the intervention (T1) and 3-month follow-up (T2) Baseline (T0), immediately after the intervention (T1), and 3-month follow-up (T2)
Secondary The change from baseline (T0) mood states assessed by Depression, Anxiety, and Stress Scale-21at immediately after the intervention (T1) and 3-month follow-up (T2) Baseline (T0), immediately after the intervention (T1), and 3-month follow-up (T2)
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