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Clinical Trials in China / NCT06853132
Recruiting Not applicable

Baduanjin With Resistance Training Program

NCT06853132 · tracked via the Priya Life Science China tracker
Sponsor
Yale University
Phase
Not applicable
Started
2025-08-30
Last updated
2025-11-21

Condition(s) studied

OsteoporosisLumbar Disc Herniation

Investigational drug(s) / intervention(s)

Baduanjin with Resistance Training Program

Baduanjin with Resistance Training Program: Baduanjin with Resistance Training Program

Study summary

The purpose of this study is to improve symptoms of Lumbar Disc Herniation (LDH) and Osteoporosis (OP) by implementing an evidence-based Baduanjin exercise to reduce pain and increase muscle strength and quality of life in Chinese patients. This study will provide new sights of exercise of elderly patients with LDH and OP for elderly patients.

Eligibility

Sex
ALL
Min age
45 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with LDH and OP based on the chart and clinical diagnostic criteria. * Age of female patients ≥ 45 years,age of male patients ≥ 50 years. * Visual analogue scale (VAS) ≥ 3 points. * Surgical operation will be performed during the 7-day admission period. * Mandarin speakers. Exclusion Criteria: * Severe primary diseases: ulcerative colitis, gastrointestinal bleeding, pancreatitis, lung cancer, pneumonia, acute respiratory distress syndrome or psychosis, depression, anxiety or substance abuse, identified by diagnosis and interview. * Current engagement in regular physical activity routines over the past 3 months: aerobic exercises for at least 30 minutes, at least 3 times per week. * Taken drugs within 3 months before enrollment: bisphosphonates, glucocorticoids, calcitonin, anticonvulsant drugs, heparin, etc.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Second Xiangya Hospital Changsha Hunan Recruiting

More Yale University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06853132 on ClinicalTrials.gov ↗ ← All trials in China