Effects of a Multimodal Telerehabilitation Program in Patients With Chronic Non-Specific Neck Pain.
1 other identifier
interventional
54
1 country
1
Brief Summary
The purpose of this study is to evaluate the clinical results in pain intensity, neck disability, range of motion, endurance deep cervical muscles, forward head position and kinesiophobia through thoracic spine mobility, deep neck muscles and thoracic strength training and pain education protocol versus a thoracic spine mobility, thoracic strength training and pain education protocol in patients with chronic non-specific neck pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2025
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
November 21, 2025
CompletedStudy Start
First participant enrolled
December 1, 2025
CompletedFirst Posted
Study publicly available on registry
December 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
ExpectedDecember 3, 2025
November 1, 2025
5 months
November 21, 2025
November 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain intensity
Measured by Visual Analogue Scale.
Baseline, 6 weeks, 1 month follow-up
Neck Disability
Measured by the Spanish version of Neck Disability Index Questionnaire.
Baseline, 6 weeks, 1 month follow-up
Secondary Outcomes (5)
Activation of deep neck flexors muscles.
Baseline, 6 weeks, 1 month follow-up
Forward head posture
Baseline, 6 weeks, 1 month follow-up
Cervical range of motion
Baseline, 6 weeks, 1 month follow-up
Kinesiophobia
Baseline, 6 weeks, 1 month follow-up
Global Rating of Change
1 month follow-up
Study Arms (2)
Experimental group
EXPERIMENTALThoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.
Control group
ACTIVE COMPARATORThoracic spine mobility, thoracic muscles strength training and pain education through telerehabilitation.
Interventions
Thoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.
Thoracic spine mobility, thoracic muscles strength training and pain education through telerehabilitation.
Eligibility Criteria
You may qualify if:
- Non-specific neck pain for at least the last 12 weeks.
- Pain intensity equal to or greater than 4 on the visual analog scale (VAS).
- Mild-moderate disability in the Neck Disability Index.
- Not reaching phase 2 in Craniocervical flexion test.
- Availability and skill to do video calls.
- Understanding Spanish.
You may not qualify if:
- Other type of neck pain.
- Previous neck surgery.
- Diagnosed metabolic diseases.
- Red flags (infection, tumors, rheumatic arthritis, or cardiovascular disease).
- History of cardio-respiratory disease that contraindicates high-intensity exercise.
- Fibromyalgia
- Pregnancy
- Physiotherapeuthic treatment continued in the last 3 month.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universitat Internacional de Cataluña
Sant Cugat del Vallès, Spain
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Daniel Pantaleon-Hernandez
Universitat Internacional de Cataluña
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Teacher in Physiotherapy
Study Record Dates
First Submitted
November 21, 2025
First Posted
December 3, 2025
Study Start
December 1, 2025
Primary Completion
May 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
December 3, 2025
Record last verified: 2025-11