Chronic Pain Clinical Trial
Official title:
Investigation of TEST (Transcranial Electric Stimulation Therapy) for Chronic Pain
NCT number | NCT05113563 |
Other study ID # | 7978 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 2, 2023 |
Est. completion date | December 2027 |
Verified date | October 2023 |
Source | New York State Psychiatric Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The goal in this study is to investigate TEST (Transcranial Electric Stimulation Therapy) for chronic pain. It requires an inpatient stay on our research unit of about a month. The study is designed to address the cognitive and emotional aspects of chronic pain and other conditions that often accompany this disorder, such as major depression or drug use.
Status | Recruiting |
Enrollment | 12 |
Est. completion date | December 2027 |
Est. primary completion date | November 2026 |
Accepts healthy volunteers | |
Gender | All |
Age group | 22 Years to 60 Years |
Eligibility | Inclusion Criteria: 1. adults (ages 22 to 60) who understand all procedures and have the ability to provide informed consent, with a score on the Mini-Mental Status Exam of at least 24; 2. participants experiencing chronic pain, with ongoing pain symptoms, and score on the Brief Pain Inventory of > 5 on question #3 (which asks about maximal pain in the past 24 hours) or > 5 on question #5 (which asks about average pain in the past 24 hours); 3. a diagnosis of chronic postoperative pain, low back pain, musculoskeletal pain, fibromyalgia, visceral pain or neuropathic pain, including complex regional pain syndrome or peripheral neuropathy; 4. no significant changes in pain medications for at least one month prior to study entry. |
Country | Name | City | State |
---|---|---|---|
United States | 1051 Riverside Drive | New York | New York |
Lead Sponsor | Collaborator |
---|---|
New York State Psychiatric Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility will be assessed by the percent of participants who complete the study | Feasibility will be assessed by the percent of participants who complete the study | 4 weeks |
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