Neural Mobilization to Improve Chronic Musculoskeletal Pain in Older Adults
Neural Mobilization in the Treatment of Chronic Musculoskeletal Pain in Older Adults: A Single-Case Experimental Design Study.
1 other identifier
interventional
4
1 country
1
Brief Summary
The goal of this clinical trial is to discover whether performing active neural mobilization exercises works to manage chronic musculoskeletal pain in older adults. The main question it aims to answer is: Can an active neural mobilization program improve pain intensity and functional capacity? Participants will:
- Perform active neural mobilization exercises for 8 weeks (twice a week), under the in-person supervision of a physiotherapist;
- Visit the clinic twice a week for 12 weeks for consultations, examinations, and symptom monitoring;
- Keep a diary of their symptoms and frequency of analgesic use.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 27, 2026
CompletedStudy Start
First participant enrolled
March 1, 2026
CompletedFirst Posted
Study publicly available on registry
March 4, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
March 4, 2026
February 1, 2026
5 months
February 27, 2026
February 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain diary
Participants will be asked to complete a daily "pain diary," recording: * Average pain intensity that day (numerical scale from 0 to 10, where 0 represents "no pain" and 10 represents "the worst pain imaginable"); * Pain-related interference that day (numerical scale from 0 to 10, where 0 represents "no interference" and 10 represents "maximum interference"); * Medication used for pain.
Every day (until the end of the study) - from week 1 to week 24
Secondary Outcomes (13)
Pain distribution
Three assessment points: 1) Baseline 2) After the 8-week intervention program 3) At the end of the study (week 24)
Neuropathic pain components
Three assessment points: 1) Baseline 2) After the 8-week intervention program 3) At the end of the study (week 24)
Pain Catastrophizing
Three assessment points: 1) Baseline 2) After the 8-week intervention program 3) At the end of the study (week 24)
Kinesiophobia
Three assessment points: 1) Baseline 2) After the 8-week intervention program 3) At the end of the study (week 24)
Signs and symptoms of hypersensitivity of the nervous system
Three assessment points: 1) Baseline 2) After the 8-week intervention program 3) At the end of the study (week 24)
- +8 more secondary outcomes
Study Arms (1)
Active Neural Mobilization Exercises
EXPERIMENTALInterventions
Participants will actively perform neural mobilization exercises for the upper and lower limbs, as well as spinal structures.
Eligibility Criteria
You may qualify if:
- Community-dwelling older adults aged 60 years or older
- People with chronic musculoskeletal pain
You may not qualify if:
- Individuals undergoing surgery in the last 3 months
- Individuals diagnosed with dementia, cancer, thrombosis, or central nervous system injury (e.g., stroke);
- Individuals who are receiving another physiotherapy intervention
- Individuals who do not understand the Portuguese language
- Individuals with mild cognitive impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Medical Sciences, University of Aveiro (Portugal)
Aveiro, 3810-193, Portugal
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 27, 2026
First Posted
March 4, 2026
Study Start
March 1, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
March 4, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share