NCT07260955

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

63
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Trial Health Score

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

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet 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 Progress87%
Dec 2025Jun 2026

First Submitted

Initial submission to the registry

November 21, 2025

Completed
10 days until next milestone

Study Start

First participant enrolled

December 1, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 3, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

December 3, 2025

Status Verified

November 1, 2025

Enrollment Period

5 months

First QC Date

November 21, 2025

Last Update Submit

November 21, 2025

Conditions

Keywords

Neck musclesChronic neck painTelerehabilitationExercise therapyPain education

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

EXPERIMENTAL

Thoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.

Other: Thoracic and neck specific exercise program and education

Control group

ACTIVE COMPARATOR

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

Other: Thoracic exercise program and education

Interventions

Thoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.

Experimental group

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

Control group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Interventions

Educational Status

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Daniel Pantaleon-Hernandez

    Universitat Internacional de Cataluña

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Daniel Pantaleon-Hernandez

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This will be a randomized controlled trial with 2 different groups.
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

Locations