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Recruiting Not applicable Interventional

Sequential and Comparative Evaluation of Pain Treatment Effectiveness Response

ClinicalTrials.gov ID: NCT04142177

Public ClinicalTrials.gov record NCT04142177. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 9:11 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CSP #2009 - Sequential and Comparative Evaluation of Pain Treatment Effectiveness Response: The SCEPTER Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

VETERANS ONLY. Chronic low back pain (cLBP) is common. Most Americans will have at least one episode of low back pain in their lifetimes. Approximately 50% of all US Veterans have chronic pain, and CLBP is the most common type of pain in this population. This study will use a sequential randomized, pragmatic, 2-step comparative effectiveness study design. The main goal is to identify the best approach for treating cLBP using commonly recommended non-surgical and non-pharmacological options. The first step compares continued care and active monitoring (CCAM) to internet-based pain self-management (Pain EASE) and an enhanced physical therapy intervention that combines Pain EASE with tailored exercise and physical activity. Patients who do not have a significant decrease in pain interference (a functional outcome) in Step 1 and those desiring additional treatment will be randomized in Step 2 to yoga, spinal manipulation therapy (SMT), or therapist-delivered cognitive behavioral therapy (CBT). Participants proceeding to randomization in Step 2 will be allowed to exclude up to one of the three Step 2 treatments based on their preferences. The investigators' primary hypothesis for the first treatment step is that an enhanced physical therapy intervention that combines pain self-management education with a tailored exercise program will reduce pain interference greater than internet-based pain self-management alone or CCAM in Veterans with cLBP. The primary outcome is change in pain interference at 3 months, measured using the Brief Pain Inventory (BPI) pain interference subscale. Study participants will be followed for one year after initiation of their final study treatments to assess the durability of treatment effects. The study plans to randomize 2529 patients across 20 centers.

Study identification

NCT ID
NCT04142177
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
2,529 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 12, 2022
Primary completion
Jun 29, 2027
Completion
Jun 29, 2027
Last update posted
May 3, 2026

2022 – 2027

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Phoenix VA Health Care System, Phoenix, AZ Phoenix Arizona 85012 Recruiting
VA Loma Linda Healthcare System, Loma Linda, CA Loma Linda California 92357-1000 Recruiting
VA Long Beach Healthcare System, Long Beach, CA Long Beach California 90822 Recruiting
VA Palo Alto Health Care System, Palo Alto, CA Palo Alto California 94304-1207 Recruiting
Rocky Mountain Regional VA Medical Center, Aurora, CO Aurora Colorado 80045 Withdrawn
Bay Pines VA Healthcare System, Pay Pines, FL Bay Pines Florida 33744-0000 Terminated
Orlando VA Healthcare System, Orlando, FL Orlando Florida 32827 Recruiting
Atlanta VA Medical and Rehab Center, Decatur, GA Decatur Georgia 30033-4004 Recruiting
Richard L. Roudebush VA Medical Center, Indianapolis, IN Indianapolis Indiana 46202-2884 Recruiting
Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD Baltimore Maryland 21201 Terminated
VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Boston Massachusetts 02130-4817 Recruiting
St. Louis VA Medical Center John Cochran Division, St. Louis, MO St Louis Missouri 63106-1621 Recruiting
VA Southern Nevada Healthcare System, North Las Vegas, NV North Las Vegas Nevada 89086 Terminated
Asheville VA Medical Center, Asheville, NC Asheville North Carolina 28805-2576 Recruiting
VA Portland Health Care System, Portland, OR Portland Oregon 97207-2964 Recruiting
South Texas Health Care System, San Antonio, TX San Antonio Texas 78229-4404 Recruiting
VA Salt Lake City Health Care System, Salt Lake City, UT Salt Lake City Utah 84148-0001 Recruiting
Hampton VA Medical Center, Hampton, VA Hampton Virginia 23667 Terminated
Hunter Holmes McGuire VA Medical Center, Richmond, VA Richmond Virginia 23249-0001 Terminated

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04142177, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2026 · Synced Sep 6, 2026

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The complete protocol, eligibility criteria, and contact information for NCT04142177 live on ClinicalTrials.gov.

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