Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
NCT06853132

Baduanjin With Resistance Training Program

Led by Yale University · Updated on 2025-11-21

110

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

Y

Yale-China Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Baduanjin With Resistance Training Program

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with Lumbar Disc Herniation and Osteoporosis based on clinical criteria
  • Female patients aged 45 years or older; male patients aged 50 years or older
  • Pain level of at least 3 on a visual analogue scale
  • Scheduled for surgical operation during the 7-day hospital admission
  • Ability to speak Mandarin
Not Eligible

You will not qualify if you...

  • Presence of severe diseases such as ulcerative colitis, gastrointestinal bleeding, pancreatitis, lung cancer, pneumonia, acute respiratory distress syndrome, psychosis, depression, anxiety, or substance abuse
  • Participation in regular aerobic exercise for at least 30 minutes, three times a week, over the past 3 months
  • Use of medications including bisphosphonates, glucocorticoids, calcitonin, anticonvulsants, or heparin within the past 3 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Second Xiangya Hospital

Changsha, Hunan, China

Actively Recruiting

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Research Team

3

3. Soohyun Nam, PhD

CONTACT

T

Tieying Qiu, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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