Brief Pain Reprocessing Therapy in Veterans

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-10

Study Completion Date

2027-06-30

Brief Summary

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This research is studying whether a Zoom-based behavioral intervention may have an impact as a treatment for Veterans with Chronic Low Back Pain (CLBP).

The study will examine:

* The acceptability of the Brief Pain Reprocessing Therapy (BPRT) intervention
* The feasibility of the BPRT intervention
* The safety of the BPRT intervention

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Detailed Description

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This study will take place remotely and there will be no on-site visits.

Conditions

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Chronic Lower Back Pain (CLBP)

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Brief Pain Reprocessing Therapy (BPRT)

Participants will have therapy over the internet.

Group Type EXPERIMENTAL

Brief Pain Reprocessing Therapy (BPRT)

Intervention Type BEHAVIORAL

Participants will have three 90-minute behavioral intervention sessions over a 3-week period, completing 35 days of brief daily assessments, and one additional set of questionnaires.

Participants will also complete study questionnaires at 1, 2, 3, and 6 months after attending the 3 behavioral intervention sessions.

Interventions

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Brief Pain Reprocessing Therapy (BPRT)

Participants will have three 90-minute behavioral intervention sessions over a 3-week period, completing 35 days of brief daily assessments, and one additional set of questionnaires.

Participants will also complete study questionnaires at 1, 2, 3, and 6 months after attending the 3 behavioral intervention sessions.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Low back pain that has lasted greater than 6 months, with pain on at least half of these days
* Must provide verification of being an Armed Service Veteran.
* Able to read, write and speak English
* Internet access and audio-conferencing capability (e.g., Zoom meetings by phone or computer) in the home

Exclusion Criteria

* Self-reported evidence of a separate medical condition (e.g., rheumatoid arthritis), acute injury in the past 12 months (e.g., self-reported spinal fracture), self-reported loss of bowel or bladder control in the past year (which may indicate presence of cauda equina syndrome), or evidence of presence of a metastasizing cancer requiring treatment
* Pending surgical procedures or interventional therapies (e.g., spinal injections) within the next 12 months
* Confirmed/suspected pregnancy
* Evidence of other conditions that may preclude participants from understanding or being able to participate in study procedure (e.g., schizoaffective disorder, suspected or diagnosed dementia)
* Currently receiving cognitive-behavioral therapy or other psychological therapies for pain
* Open litigation in the past 1 year, as assessed in preliminary study screening.
* Any other diseases or conditions that would make a patient unsuitable for study participation as determined by the site principal investigators.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No