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The Added Value of a Behavioral Weight Reduction Program to Blended Rehabilitation in Patients With Chronic Low Back Pain: A Randomized Clinical Trial
We will recruit overweight/ obese participants between the age of 18 and 65 with chronic nonspecific low back pain . The participants will be randomly assigned to one of two interventions (each lasting 10 weeks). All interventions will be delivered in a blended format and will be a combination of online education material and face-to-face sessions with a physical therapist. The first group (experimental intervention) will receive a behavioral weight reduction program combined with pain neuroscience education plus cognition-targeted exercise therapy. Participants in the second group (control intervention) will receive pain neuroscience education and cognition-targeted exercise therapy alone. Allocation to the groups will be at random. Participants and assessors will be blinded for group allocation. The primary outcomes is pain intensity. Secondary outcomes include other pain related outcomes, body composition, physical activity, sedentary behavior, dietary intake and function.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Vrije Universiteit Brussel
Brussels, Belgium
Rotterdam University of Applied Sciences
Rotterdam, Netherlands
Start Date
May 1, 2025
Primary Completion Date
December 1, 2026
Completion Date
December 1, 2026
Last Updated
May 25, 2025
84
ESTIMATED participants
Pain Neuroscience Education
BEHAVIORAL
Cognition-targeted exercise therapy
BEHAVIORAL
Behavioral weight reduction program
BEHAVIORAL
Lead Sponsor
Vrije Universiteit Brussel
Collaborators
NCT05508360
NCT07160400
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT07150962