NCT07449819

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4

participants targeted

Target at below P25 for not_applicable

Timeline
2mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress54%
Mar 2026Aug 2026

First Submitted

Initial submission to the registry

February 27, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

March 1, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 4, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

March 4, 2026

Status Verified

February 1, 2026

Enrollment Period

5 months

First QC Date

February 27, 2026

Last Update Submit

February 27, 2026

Conditions

Keywords

chronic musculoskeletal painolder adultsphysical therapyneural mobilization

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

EXPERIMENTAL
Other: Active Neural Mobilization Exercises

Interventions

Participants will actively perform neural mobilization exercises for the upper and lower limbs, as well as spinal structures.

Active Neural Mobilization Exercises

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

Central Study Contacts

Frederico M Baptista

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: The experimental methodology selected to address the objectives of this study was a single-case experimental design (SCED) with multiple baseline design (MBD). Participants will alternate between three sequential phases: Phase A - baseline, Phase B - experimental phase, and Phase A' - follow-up. Phase B will have the same duration for all participants, while Phases A and A' will have different durations for each participant.
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

Locations