Feasibility and Acceptability of Group Pain Reprocessing Therapy for Veterans With Chronic Neck/Back Pain
NCT ID: NCT06406699
Last Updated: 2025-07-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
46 participants
INTERVENTIONAL
2024-04-17
2025-02-08
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Experiential Avoidance in Combat Veterans With and Without Posttraumatic Stress Disorder
NCT01652430
Self-monitoring and Reflection's Impact on Psychotherapy Outcomes: A Trial Protocol.
NCT06038747
EEG Biofeedback in the Treatment of Chronic Treatment-Resistant PTSD
NCT01259921
A Trial of Group Psychotherapy for Veterans and Military Personnel With Post Traumatic Stress Disorder (PTSD)
NCT00984698
Suicide and Trauma Reduction Initiative Among VEterans
NCT03933059
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Pain Reprocessing Therapy
Participants will participate in once weekly telehealth group pain reprocessing therapy. Sessions will last approximately 1 hour in length. Group size will be approximately 10 individuals.
Pain Reprocessing Therapy (PRT)
PRT is a psychological intervention for chronic pain patients with a primary nociplastic component. PRT aims to help patients reconceptualize their pain as a non-dangerous signal that is not indicative of tissue pathology or structural abnormality. Through decreasing the threat level of their chronic pain, the pain itself can also resolve.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pain Reprocessing Therapy (PRT)
PRT is a psychological intervention for chronic pain patients with a primary nociplastic component. PRT aims to help patients reconceptualize their pain as a non-dangerous signal that is not indicative of tissue pathology or structural abnormality. Through decreasing the threat level of their chronic pain, the pain itself can also resolve.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Able to attend at least 7/8 telehealth group sessions
* Access to safe living space, quite room, reliable internet, and electronic device that can be used to attend telehealth therapy sessions.
Exclusion Criteria
* Suicide attempt, SI, HI, or inpatient psychiatric hospitalization in the past 5 years
* Not receiving/has not received disability or workers compensation related to back pain in the past 2 years.
* Is not currently involved in litigation regarding chronic back pain.
* Current misuse or overuse of alcohol or drugs
* Major surgery or other major medical events in the next 6 months
* Known vertebral/spinal fracture or tumor.
* Back surgery within last 2 years
* Difficulty controlling bowel movements
* Current or recent diagnosis of cancer
* Current or recent diagnosis of severe cardiovascular disease
* Unexplained or unintended greater than 20 pound weight loss in the past year
* Diagnosis of rheumatoid arthritis, polymyalgia rheumatica, scleroderma, Lupus, polymyositis, or other specific inflammatory disorders
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
VA Eastern Colorado Health Care System
FED
University of Colorado, Denver
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Colorado - Anschutz Medical Campus VA
Aurora, Colorado, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
23-1387
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.