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A Comparison of Two Brief Interventions for People With Chronic Low Back Pain

A Comparison of Two Brief Interventions for People With Chronic Low Back Pain

Non Recruiting
18 years and older
All
Phase N/A

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Overview

The goal is to undertake a Decentralized Randomized Pilot Feasibility study to inform the methods for a definitive Randomized Controlled Trial (RCT) (including recruitment success, participant experience, intervention delivery, safety, outcome measurement and sample size estimation). The main question is if the methods used are feasible for an adequately powered future RCT. Participants will be randomly allocated to receive either: Intervention - OldPain2Go® treatment or Placebo Control - Jacobson's progressive relaxation

Description

The project is a virtual Randomized Control Trial and the independent variable is OldPain2Go® a novel brief intervention for people with chronic low back pain. The investigators aim to answer the research question: Is OldPain2Go® an effective intervention for pain and function in people with chronic low back pain - when applied in an adequately powered RCT comparing OldPain2Go® with placebo? The Intervention arm participants will receive OldPain2Go® and the Control arm participants will receive Jacobson's progressive relaxation, as a placebo. The Control (placebo) is a commonly used element of treatment, for a wide range of conditions, but is never applied only once (or twice) as a treatment.

Eligibility

Inclusion Criteria:

  • Currently suffering from persistent, non-specific, low back pain of six or more months duration
  • No known tissue damage, structural abnormality, or pathology causing persistent low back pain
  • Aged over 18 years
  • Person's for whom Oldpain2go® is indicated as a treatment option, after the standard clinical screening process for the Oldpain2go® treatment
  • Has access to digital communication device able to host encrypted secure on-line meetings.

Exclusion Criteria:

  • Any Red Flags,
  • Any causative (or potentially causative) structural abnormality, or pathology detected or suspected
  • Any concurrent pathology, or condition that would render them unsuitable for on-line virtual assessment and Physiotherapy treatment
  • Lack of (or any reason to doubt presence of) Mental Capacity to give Informed Consent

Study details
    Low Back Pain

NCT06218459

Teesside University

21 October 2025

FAQs

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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