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Thymalin

Thymulin, Thymic Factor, Serum Thymic Factor, Facteur Thymique Serique

Quick Stats
Studies 202
Trials 37
Completed NA INTERVENTIONAL NCT05397535

Baduanjin Lower Elevated Blood PreSsure Study

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The aim of this study is to evaluate the effects of Baduanjin on blood pressure in individuals with high normal blood pressure (SBP 130-139 mmHg, and/or DBP 85-89 mmHg), as well as on glucose and lipid metabolism, quality of life, psychology, exercise, immune inflammation, endothelial function, and arterial stiffness.

Interventions

Name: Baduanjin
Type: BEHAVIORAL
Description: Participants in Baduanjin group will receive health education on hypertension and attend a 4-hour class to learn Baduanjin before receiving the interventions after the randomization. Baduanjin exercise protocol is based on the "Fitness Qigong Baduanjin Standard" enacted by the General Administration of Sports in 2003. Each Badaunjin exercise session will last at least 30 minutes and be conducted at least 5 days per week for 52 weeks. These participants will be required to practice Baduanjin regularly, and the researchers will monitor their adherence to practice and provide reminders if needed.
Name: Brisk walking
Type: BEHAVIORAL
Description: Participants in this group will receive health education on hypertension and practice brisk walking on their own for at least 30 minutes, at least 5 days per week for 52 weeks. These participants will be required to do brisk walking regularly, and the researcher will monitor their adherence to practice and provide reminders if needed.

Primary Outcomes

Measure: Change from baseline ambulatory 24-h systolic blood pressure (mmHg) at 12 week
TimeFrame: Baseline, 12 week
Description: Change form Baseline ambulatory 24-h systolic blood pressure at 12 week will be measured by ambulatory blood pressure monitoring to investigate the short-term antihypertensive effect of Baduanjin.
Measure: Change from baseline ambulatory 24-h systolic blood pressure (mmHg) at 52 week
TimeFrame: Baseline, 52 week
Description: Change from baseline ambulatory 24-h systolic blood pressure at 52 week will be measured by ambulatory blood pressure monitoring to investigate the long-term antihypertensive effect of Baduanjin.

Trial Information

NCT ID

NCT05397535

Status

Completed

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

China National Center for Cardiovascular Diseases

Last Updated

December 15, 2025