Personalized vs. standard back pain rehab: which works better for seniors?
NCT ID NCT07699419
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study compares two types of physical therapy for adults aged 60 and older with chronic low back pain. One approach tailors exercises to each person's specific physical problems, while the other uses a standard program to improve overall function. The goal is to see which method is more practical and effective for reducing pain and improving daily activities.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- physical therapy (impairment-based treatment or functional restoration program)
- What this could lead to
- If one approach proves better, it could lead to more effective, personalized rehabilitation for older adults with chronic back pain.
- What could go wrong
- This is a small feasibility study with only 18 participants, so results may not apply to everyone. The trial tests practicality, not yet effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 18 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ≥ 60 years * Chronic Non-Specific Low Back Pain (CNSLBP) * Pain duration ≥ 12 weeks * No identifiable specific spinal pathology * Pain Location * Pain localized between the 12th rib and gluteal folds * With or without non-dermatomal referred pain not extending below the knee * Pain Intensity * Mean pain intensity ≥ 4/10 on the Numeric Rating Scale (NRS) over the past 7 days * Functional Disability * Oswestry Disability Index (ODI) ≥ 20% (moderate disability or higher) * Mechanical Pain Characteristics * Presence of ≥ 2 of the following: * Pain aggravated by movement, loading, or prolonged postures * Pain relieved by rest or positional change * Morning stiffness \< 30 minutes * Absence of constant, non-mechanical night pain Functional Capacity * Able to ambulate independently (with or without assistive device) * Able to actively participate in an exercise-based rehabilitation program * Clinical Stability * Stable medication regimen (analgesics, anti-inflammatories, or related drugs) for ≥ 4 weeks * No planned changes in pharmacological treatment during the study period * Cognitive \& Communication Ability * Able to understand study procedures and follow instructions * MMSE ≥ 24 (or equivalent cognitive screening) * Consent * Provides written informed consent Exclusion Criteria: * 1\. Specific Spinal Pathology ("Red Flags") * Suspected or confirmed: * Spinal fracture * Malignancy * Spinal infection * Inflammatory spondyloarthropathy Clinical indicators: Unexplained weight loss Fever or systemic illness History of significant trauma 2\. Radicular or Neurological Involvement * Radiculopathy defined by ANY of: * Dermatomal pain radiating below the knee * Progressive motor weakness * Objective neurological deficit (sensory, reflex, or motor) 3\. Lumbar Spinal Stenosis (Severe) * Neurogenic claudication limiting walking to \< 100 meters, OR * Symptoms not relieved by rest or flexion 4\. Prior Surgical or Structural Conditions Lumbar spine surgery within the past 12 months 5\. Medical Contraindications to Exercise * Severe osteoporosis with high fracture risk * Uncontrolled cardiovascular, respiratory, or metabolic disease * Any condition precluding safe participation in rehabilitation 6\. Cognitive or Behavioral Barriers * Severe cognitive impairment (MMSE \< 24) * Inability to comply with study procedures 7\. Confounding Treatment Factors * Participation in structured physiotherapy or rehabilitation within the past 3 months * Planned concurrent rehabilitation during the study 8\. Psychosocial Confounders Ongoing litigation or compensation claims related to low back pain
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Recovery City Clinic
Cairo, Cairo Governorate, Egypt
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