Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Mindfulness training using virtual reality for veterans with spinal cord injuries

Official title: Exploring Virtual Reality Mindfulness Training for Veterans With SCI and Chronic Pain

Run by VA Office of Research and Development · NCT06587607 · Data updated 2026-11-12

This study is testing a virtual reality mindfulness program to see if it can help veterans with spinal cord injuries manage pain better and improve their quality of life.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment10 (estimated)
SponsorVA Office of Research and Development
Federal
Locations1 site (Houston, Texas)
StatusRecruiting
StartedJuly 1, 2025
Main results expectedJune 30, 2027
Study endsJune 30, 2027
Registry record updatedMarch 2, 2026
Trial IDNCT06587607 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are veterans aged 18 and older with a diagnosis of spinal cord injury and chronic pain.

Probably not a fit

Patients who are unable to consent for research or medical care will 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 study aims to adapt a mindfulness program called VA Compassionate Awareness Learning Module (VA CALM) for veterans with spinal cord injuries (SCI) by first assessing the program's accessibility and acceptability. Initially, the unmodified curriculum will be delivered to a group of veterans with SCI to identify necessary accommodations. Following this, a steering committee will develop tailored modifications, and the modified program will be delivered via virtual reality to evaluate its feasibility and acceptability. The ultimate goal is to improve chronic pain management and enhance the quality of life for veterans with SCI.

Why it matters

Potential benefit: If successful, this program could significantly improve chronic pain management and overall well-being for veterans with spinal cord injuries.

How similar studies have gone: While the use of virtual reality for mindfulness training is a growing field, this specific adaptation for veterans with spinal cord injuries is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Veteran
* Diagnosis of spinal cord injury with incomplete or complete tetraplegia based on AIS score OR incomplete or complete paraplegia based on AIS score.
* Endorses chronic pain lasting 3 months;
* age 18+ years
* Access to high-speed internet
* Endorse being (at least) minimally proficient on the computer (eg, able to check emails, read the news, etc.); be able, either independently or with caregiver support, to get online for virtual meetings and don/doff VR equipment
* Able to speak clearly and independently to participate in focus group interviews.

Exclusion Criteria:

-Individuals unable to consent for research or medical care are ineligible to participate.

Where it's running

  • Michael E. DeBakey VA Medical Center, Houston, TX
    Houston, Texas, United States
    Recruiting

Study contacts

  • Principal investigator: Hilary Touchett, PhD MSN BSN — Michael E. DeBakey VA Medical Center, Houston, TX
  • Study coordinator: Hilary Touchett, PhD MSN BSN
  • Email: hilary.touchett@va.gov
  • Phone: (713) 791-1414

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.