Virtual Reality Guided Acupuncture Imagery Treatment for Chronic Low Back Pain (NCT06814470) | Clinical Trial Compass
CompletedNot Applicable
Virtual Reality Guided Acupuncture Imagery Treatment for Chronic Low Back Pain
United States31 participantsStarted 2024-07-16
Plain-language summary
Testing the effect of Virtual Reality - guided imagery acupuncture
Who can participate
Age range18 Years – 75 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Volunteers 18-75 years of age.
* Meet the Classification Criteria of chronic LBP (having low back pain for more than 6 months), as determined by the referring physician.
* At least 4/10 clinical pain on the 11-point LBP intensity scale.
* Must have had a prior evaluation of their low back pain by a health care provider, which may have included radiographic studies. Documentation of this evaluation will be sought from Partners or outside medical records and kept in the subject's research record.
* At least a 10th grade English-reading level; English can be a second language provided that the patients feel they understand all the questions used in the assessment measures.
Exclusion Criteria:
* Specific causes of back pain (e.g. cancer, fractures, infections),
* Complicated back problems (e.g. prior back surgery, medico legal issues),
* Possible contraindications for acupuncture (e.g. coagulation disorders, cardiac pacemakers, pregnancy, seizure disorder), and conditions that might confound longitudinal effects or interpretation of results (e.g. severe fibromyalgia, rheumatoid arthritis).
* Conditions making study participation difficult (eg, paralysis, psychoses, or other severe psychological problems as per the judgment of a study investigator during Session 1)
* The intent to undergo surgery during the time of involvement in the study.
* Unresolved medical legal/disability/workers compensation claims in connection with low back pain.
* Lacking the cap…
What they're measuring
1
Retention
Timeframe: Through study intervention, an average of about four weeks
2
Satisfaction to the Interventions
Timeframe: up to 4 weeks
3
Number of Adverse Events (Safety of the Intervention)
Timeframe: Through study interventions, an average of about four weeks