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Clinical Trials/NCT06307483
NCT06307483
Completed
Not Applicable

Dose-effect Relationship of Tai Chi on Health Promotion in Different Age Groups

Beijing Sport University1 site in 1 country499 target enrollmentAugust 25, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Disorder
Sponsor
Beijing Sport University
Enrollment
499
Locations
1
Primary Endpoint
Pittsburgh Sleep Quality Index
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to investigate the physical and mental health status of middle-aged and elderly people of different ages and practicing Tai chi for different periods of time, so as to provide a strong theoretical basis and practical guidance for delaying age-related aging and preventing and treating the occurrence and development of chronic diseases.

Registry
clinicaltrials.gov
Start Date
August 25, 2023
End Date
November 25, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Beijing Sport University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men and women aged 20-79 years.
  • People who practice Tai chi for a long time.
  • People with long-term exercise habits.
  • People who have no habit of exercising.

Exclusion Criteria

  • People currently participating in other interventions (e.g., nutrition, psychological, exercise, health education).
  • People with cognitive impairment and movement disorders.
  • Cardiovascular and cerebrovascular events (physician-diagnosed heart disease, such as coronary heart disease, hypertensive heart disease, acute myocarditis, pulmonary heart disease, etc.) in the past 6 months.
  • People with other serious chronic diseases, such as asthma, cancer, chronic heart failure, severe depression, or other mental disorders.

Outcomes

Primary Outcomes

Pittsburgh Sleep Quality Index

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

With subscale scores ranging from 0 to 3, the PSQI assesses subjective sleep quality in the previous month and consists of seven items (sleep duration, sleep latency, sleeping medications, sleep disturbance, daytime dysfunction, sleep quality, and sleep efficiency). The total score of the PSQI, ranging from 0 to 21, is the sum of subscale scores, and the higher the scores, the lower the subjective quality of sleep.

Heart rate variability (HRV)

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

HRV, a non-invasive method used to evaluate the autonomic nervous system modulation on the cardiac sinus node, describes the oscillations between consecutive electrocardiogram R-R intervals. High levels of HRV indices are generally signs of efficient autonomic mechanisms that characterise a healthy individual, while low or reduced HRV often show an autonomic nervous system malfunction and may imply health impairment.

Cardiac Output (CO)

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

Cardiac Output (CO) is a key indicator in echocardiographic examinations, used to measure the total volume of blood pumped by the heart per minute. This parameter reflects the efficiency of the heart's pumping action and the status of systemic blood circulation. The measurement of Cardiac Output is based on the volume of blood ejected by the heart with each beat (stroke volume) and the number of heartbeats per minute. Cardiac Output is typically expressed in liters per minute (L/min).

The Berg Balance Scale(BBS)

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

The BBS scale evaluates an individual's ability to maintain their balance while performing functional activities. It includes 14 items and each section is scored between 0 (worst) and 4 (best), and measures level of dependence/independence in positions such as standing from sitting, standing with feet together, standing in full balance position, balancing on one leg, as well as ability to change positions. High BBS score indicates good balance. Participants are classifed based on BBS score as high fall risk, balance disorder (0-20 points), moderate fall risk, acceptable balance (21-40 points), and low fall risk, good balance (41-56 points)

The 30-s Chair Stand Test

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

In the 30-s CST, which assesses dynamic balance and physical ftness, the individual sits in the middle of a chair with seat height of 43 cm, with a straight back, feet fat on the foor, and arms crossed over the chest with hands at shoulder level. The test starts with the subject in this position at the "go" command. The number of times the patient rises to a full standing position without assistance in 30 s is recorded as the test score. A score of 5 indicates strength and 10 indicates both strength and endurance

Lower limb muscle strength test

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

Using the micro FET3 (HOGGAN, USA) to test lower limb muscle strength. The main muscles tested include the tibialis anterior, triceps surae, quadriceps femoris, hamstrings, and iliopsoas. Each muscle is tested twice, and the maximum value is recorded

Flow-mediated dilation (FMD)

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

Flow-mediated dilation (FMD) can assess endothelium-dependent vasodilation, evaluating vascular elasticity and dilation function. Its mechanism involves inducing reactive hyperemia, increasing arterial blood flow, leading to elevated shear stress on the vessel wall, prompting endothelial cells to release NO, resulting in vasodilation. A normal FMD value is ≥7%; values \<4% indicate endothelial dysfunction.

Intima-Media Thickness (IMT)

Time Frame: This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months

Intima-Media Thickness (IMT) is a significant indicator measured through carotid ultrasound examination, used to assess the thickness of the carotid artery wall. The measurement of IMT focuses on the distance between the intima and media layers of the carotid artery, serving as a key indicator of early changes in atherosclerosis.

Secondary Outcomes

  • Hand Grip Strength(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • HUR Labs Balance Software Suite(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Finger-Ring Test(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Body Fat Percentage(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Shape Trail Test (STT)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Short-Physical Performance Battery (SPPB)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Hospital Anxiety and Depression Scale (HADS)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Star Excursion Balance Test apparatus(SEBT)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Upper and Lower Body Flexibility(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • The SARC-F scale(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • 1-back Task more-odd shifting Task Stroop Task(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Timed Up and Go(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Single-leg stance with eyes closed(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Ankle-Brachial Index (ABI)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • E/A ratio(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Close-eyed stepping in place(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Blood pressure variability (BPV)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Brachial-ankle pulse wave velocity (BaPWV)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)
  • Montreal Cognitive Assessment(MoCA)(This study was a cross-sectional study. Each subject was measured only once from the day of randomization to the first assessment, assessed up to 3 months)

Study Sites (1)

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