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Clinical Trials in Spain / NCT07260955
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Effects of a Multimodal Telerehabilitation Program in Patients With Chronic Non-Specific Neck Pain.

NCT07260955 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2025-12
Last updated
2025-12-03

Condition(s) studied

Chronic Neck PainNon-specific Neck Pain

Investigational drug(s) / intervention(s)

Thoracic exercise program and educationThoracic and neck specific exercise program and education

Thoracic exercise program and education: Thoracic spine mobility, thoracic muscles strength training and pain education through telerehabilitation.

Thoracic and neck specific exercise program and education: Thoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Universitat Internacional de Cataluña Sant Cugat del Vallès Spain

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07260955 on ClinicalTrials.gov ↗ ← All trials in Spain