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Recruiting NCT06641102

Healing Track Clinical Trial

No phase Interventional Chronic Back Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Self-Guided Program (Tier 1), Coach Assisted Program (Tier 3), Standard of Care (SOC).
Who it may be relevant to
Registry conditions: Chronic Back Pain. Basic parameters: 21 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Healing Track Randomized Clinical Trial

Overview

This is a randomized clinical trial to evaluate a digital pain reprocessing therapy (PRT) intervention for chronic back pain (CBP). The purpose of this research is to test whether a new digital treatment for chronic pain works as well as traditional treatments for chronic back pain (CBP). Some people with CBP experienced side effects from other treatments, or previous treatments did not relieve pain, so this research aims to see if a digital therapy is a better option for CBP. This study will assess changes in pain intensity from PRT intervention compared to a standard of care (SOC) control group in adults with CBP. SOC is defined as a comprehensive clinical care plan, including a consultation with physiatrist and prescribed interventions, which will capture a comparison representative of all potential interventions that are recommended for an individual. The research team plans to enroll 180 participants who will be randomized into one of three groups.

Interventions

  • Other Self-Guided Program (Tier 1)
    The study intervention is a smartphone application. Tier 1: self-guided program, includes videos, guided meditations, and worksheets that are delivered to users in 10 different topical modules. Two modules are delivered per week, with email reminders. It will emphasize that PRT is a practice that requires users to come back to the material regularly to help retrain the brain often (just like how you need to practice and complete exercises between PT sessions).
  • Other Coach Assisted Program (Tier 3)
    The study intervention is a smartphone application. Tier 3: one-on-one coaching program that sets users up with trained PRT coaches who will walk them through the program individually. Users will meet with the assigned coaches once per week for an hour-long Zoom-hosted session that covers the same information as Tier 1, however in a completely personal and individualized way, focusing on the content that is most relevant for the user/patient at the time of the session. Tier 3 users will also re
  • Other Standard of Care (SOC)
    SOC is defined as a comprehensive clinical care plan, including a consultation with physiatrist and prescribed interventions, which will capture a comparison representative of all potential interventions that are recommended for an individual.

Primary outcome measures

  • Brief Pain Inventory Short Form [Time frame: <Day 0, Day 0, Day 1, Week 6, Week 10, Month 8.5]

Eligibility criteria

Inclusion criteria

  • Aged 21 to 70
  • Chronic Back Pain- CBP will be defined according to the criteria established by a recent NIH task force
  • Pain duration must be at least 3 months, with back pain being an ongoing problem for at least half the days of the last 6 months. That is, patients can meet criteria by either reporting pain every day for the past 3 months, or by reporting pain on half or more of the days for the past 6+ months.
  • Patients must rate pain intensity at 4/10 or greater on the Brief Pain Inventory-Short Form (BPISF) (on the item measuring average pain over the last week).
  • Participants must also be comfortable and able to communicate via email or text message, as several study measures are collected in this manner.
  • Able to use a smartphone

Exclusion criteria

  • Back pain associated with compensation or litigation issues as determined by self-report within the past year
  • Leg pain is greater than back pain, as this suggests neuropathic pain, which may be less responsive to psychotherapy
  • Cauda Equina syndrome, as screened for by self-reported inability to control bowel or bladder function
  • Self-reported diagnoses of schizophrenia, multiple personality disorder, or dissociative identity disorder
  • Self-reported use of intravenous drugs, due to concerns about infections and subject compliance with experimental protocols

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Icahn School of Medicine at Mount Sinai - Abilities Research Center — New York

Identifiers

NCT: NCT06641102 · STUDY-24-00080

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗