Phantom Limb Clinical Trial
Official title:
Psychosocial and Visual Feedback Intervention for Phantom Limb Pain
Verified date | October 2019 |
Source | VA Office of Research and Development |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this study is to test whether a combination of cognitive-behavior therapy and mirror training reduces phantom limb pain for veterans with amputations.
Status | Completed |
Enrollment | 59 |
Est. completion date | December 2012 |
Est. primary completion date | September 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - Adult (21or over) - unilateral amputation at or above wrist or ankle - phantom limb pain occurring at least weekly - living within 50 miles of a recruitment site (San Diego, San Francisco, or Long Beach VAs). - able to read and speak English Exclusion Criteria: - Current alcohol or drug dependence - active psychosis - medical problems that preclude participation - current enrollment in behavioral pain management |
Country | Name | City | State |
---|---|---|---|
United States | VA Medical Center, Long Beach | Long Beach | California |
United States | VA San Diego Healthcare System, San Diego | San Diego | California |
United States | VA Medical Center, San Francisco | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Phantom Limb Pain Questionnaire | The primary outcome measure is the severity of phantom limb pain on a likert scale from 0 (no pain) to 10 (worst pain imaginable) | Baseline, each weekly treatment session (1-8), 12 weeks post treatment, 24 weeks posttreatment. | |
Secondary | Short Form-12 (SF-12) | the Short Form-12 (SF-12) is a standardized self-report questionnaire that assesses mental and physical functioning. The Physical Component Summary (PCS) is scored on a scale from 0-100, with higher scores representing better reported health. | Baseline, end of treatment (8 weeks after baseline) |
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