Effectiveness Study of an Exercise Program for Older Adults With Chronic Musculoskeletal Pain
NCT ID: NCT06667830
Last Updated: 2025-10-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
70 participants
INTERVENTIONAL
2024-10-31
2026-02-28
Brief Summary
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What is the impact of the intervention program on participants´ pain intensity (primary outcome), function, physical performance, and somatosensory function (secondary outcomes)? Participants will be assessed at 3 different moments: initial assessment (T0), at the end of the intervention protocol (10 weeks) (T1) and 3 months after the end of the intervention protocol (T2). The intervention protocol will consist of a multimodal exercise program to be carried out over a period of 10 weeks at a frequency of twice a week.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Physical exercise
Physical exercise program
The physical exercise program will consist of exercises from three different exercise modalities: aerobic training, balance exercises, and isometric exercises.
Physical exercise + Neural mobilization
Physical exercise program
The physical exercise program will consist of exercises from three different exercise modalities: aerobic training, balance exercises, and isometric exercises.
Neural mobilization techniques
Neural mobilization techniques for the upper and lower quadrants will be actively performed by participants.
Interventions
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Physical exercise program
The physical exercise program will consist of exercises from three different exercise modalities: aerobic training, balance exercises, and isometric exercises.
Neural mobilization techniques
Neural mobilization techniques for the upper and lower quadrants will be actively performed by participants.
Eligibility Criteria
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Inclusion Criteria
* People with primary or secondary chronic musculoskeletal pain in any body site
* People able to walk independently
Exclusion Criteria
* Patients with a self-reported diagnoses of infection diseases, dementia, tumor/cancer, stroke, uncontrolled diabetes, or at high risk of developing cardiovascular events
* Those with physical limitations that make it impossible for them to carry out the intervention protocols independently (e.g., wheelchair user)
* Patients who are receiving another physical therapy intervention to treat their pain.
60 Years
ALL
No
Sponsors
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Aveiro University
OTHER
Responsible Party
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Frederico Mesquita Baptista
Principal Investigator
Locations
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Department of Medical Sciences (University of Aveiro), Campus Universitário de Santiago, Agra do Crasto, Edifício 30
Aveiro, , Portugal
Countries
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Other Identifiers
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RCT2
Identifier Type: -
Identifier Source: org_study_id
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