Clinical trial Recruiting at 1 site Interventional Ages 40 to 100

Improving physical function in veterans with COPD and chronic pain through walking and Tai Chi

Official title: The Effect of a Technology-Mediated Integrated Walking and Tai Chi Intervention on Physical Function in Veterans With COPD and Chronic Musculoskeletal Pain

Run by VA Office of Research and Development · NCT05701982 · Data updated 2026-11-12

This study is testing if a program that combines walking and Tai Chi can help veterans with COPD and chronic pain improve their physical abilities and overall well-being.

Quick facts

Study typeInterventional
Ages40 Years to 100 Years
SexAll
Enrollment136 (estimated)
SponsorVA Office of Research and Development
Federal
Drugs / interventionschemotherapy, radiation
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedJanuary 3, 2024
Main results expectedSeptember 30, 2027
Study endsMarch 31, 2028
Registry record updatedJanuary 22, 2026
Trial IDNCT05701982 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are veterans aged 40 and older with a clinical diagnosis of COPD and a pain score greater than 3 for more than three months.

Probably not a fit

Patients who do not have access to the necessary technology for participation or those with severe mobility limitations may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to evaluate the effectiveness of a technology-mediated intervention combining walking and Tai Chi to enhance physical function in veterans suffering from chronic obstructive pulmonary disease (COPD) and chronic musculoskeletal pain. The intervention, known as Every Step Counts (ESC), utilizes a web-based platform and pedometer to set personalized activity goals and provide feedback, education, and social support. By integrating Tai Chi, which is known for its benefits in pain management, the study seeks to address the barriers to physical activity faced by this population. The research is designed to improve health-related quality of life by reducing the burden of disease and maximizing functional capabilities in veterans with chronic conditions.

Why it matters

Potential benefit: If successful, this intervention could significantly improve physical function and quality of life for veterans with COPD and chronic pain.

How similar studies have gone: Previous studies have shown success with similar technology-mediated interventions for increasing physical activity in COPD patients, making this approach promising.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male and female participants, aged 40 and older
* Clinical diagnosis of COPD defined as history of cigarette consumption of \> 10 pack-years, and either a ratio of forced expiratory volume in one second (FEV1) to forced vital capacity (FVC) \< 0.70 or chest computerized tomography (CT) evidence of emphysema\*
* Numeric Rating Scale pain score \> 3 for \> 3 months
* Self-reported ability to walk a minimum of one block, bend at the hip, and transfer weight from one leg to another
* Ability to complete 800 feet walk with Fitbit Inspire-2 recording \> 90% accuracy to detect steps compared to manual counts\*
* Have access to a computer or smartphone with Internet connection or willing to come to study site to use study computers
* Have access to videoconferencing audio and video capabilities
* Competent to provide informed consent and willingness to make return study visits

  * Different criteria are used if baseline study visit is a virtual one.

Exclusion Criteria:

* COPD exacerbation in the previous 1 month
* Clinical signs of unstable cardiovascular disease (active coronary artery disease, congestive heart failure, uncontrolled atrial fibrillation, or uncontrolled hypertension)
* Oxygen saturation \< 85% recorded on baseline 4-meter walk\*
* High fall risk (unable to perform 5 chair stand tests)
* Inability to ambulate
* Inability to complete questionnaires
* Inability to collect at least 7 of 10 days of baseline step counts
* Active substance abuse
* Participation in a regular exercise (i.e., MOVE! or Gerofit) or Tai Chi program in the previous 3 months
* Concurrent participation in another interventional research study
* Receipt of hospice or end-of-life palliative care
* Active medical intervention that would cause a meaningful increase in pain such as surgery, chemotherapy, or radiation therapy

  * Different criteria are used if baseline study visit is a virtual one.

Where it's running

  • VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
    Boston, Massachusetts, United States
    Recruiting

Study contacts

  • Principal investigator: Marilyn L. Moy, MD — VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
  • Study coordinator: Marilyn L Moy, MD
  • Email: Marilyn.Moy@va.gov
  • Phone: (857) 203-6622

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.