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Not yet recruitingNCT07260955Updated Dec 3, 2025

Effects of a Multimodal Telerehabilitation Program in Patients With Chronic Non-Specific Neck Pain.

An interventional study of Thoracic exercise program and education and Thoracic and neck specific exercise program and education in Chronic Neck Pain and Non-specific Neck Pain, sponsored by Universitat Internacional de Catalunya. Not yet recruiting at 1 site in Spain. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-12-03.

Sponsored by Universitat Internacional de Catalunya · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2026, 5 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

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.

Read the detailed description

The cervical spine is the most mobile region of the spine and must be strong enough to support the weight of the skull and thoracic spine is the most stiff region. In addition, patients often catastrophize their pain, it has a major impact on quality of life. Strength deficits of the deep cervical muscles are related to different clinical conditions, such as non-specific neck pain. Training and education protocols can help to improve pain, function, posture and cross-sectional area. However, there are no multimodal protocols in subjects with chronic non-specific neck pain including deep neck extensor and flexor muscles, thoracic spine mobility and pain education.

02

Conditions studied

  • Chronic Neck Pain
  • Non-specific Neck Pain

Keywords

  • Neck muscles
  • Chronic neck pain
  • Telerehabilitation
  • Exercise therapy
  • Pain education
03

In context

Lead sponsor

Universitat Internacional de Catalunya is the lead sponsor of 144 studies on the registry; 43 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts 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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
54 participants (estimated)

Study arms

  • Experimental
    Experimental group

    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

  • Active comparator
    Control group

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

    Other: Thoracic exercise program and education

Interventions

  • OtherThoracic exercise program and education

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

  • OtherThoracic 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.

06

What researchers measure

Primary outcomes

  1. Pain intensity

    Measured by Visual Analogue Scale.

    Time frame: Baseline, 6 weeks, 1 month follow-up

  2. Neck Disability

    Measured by the Spanish version of Neck Disability Index Questionnaire.

    Time frame: Baseline, 6 weeks, 1 month follow-up

Secondary outcomes

  1. Activation of deep neck flexors muscles.

    Measured by Cranio-cervical flexion test

    Time frame: Baseline, 6 weeks, 1 month follow-up

  2. Forward head posture

    Measured by craniovertebral angle.

    Time frame: Baseline, 6 weeks, 1 month follow-up

  3. Cervical range of motion

    Measured by CROM(Cervical Range-of-Motion Instrument). Cervical flexion, extension, right/left side bending and right/left rotation.

    Time frame: Baseline, 6 weeks, 1 month follow-up

  4. Kinesiophobia

    Measured with Spanish version of Tampa Scale

    Time frame: Baseline, 6 weeks, 1 month follow-up

  5. Global Rating of Change

    Measured by Global Rating of Change Scale

    Time frame: 1 month follow-up

07

Study locations

1 site
  • Universitat Internacional de Cataluña
    Sant Cugat del Vallès, Spain
    • Universitat Internacional de Cataluña · Contact · nnogales@uic.es · 935042000
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07260955
Lead sponsor
Universitat Internacional de Catalunya
Responsible party
Daniel Pantaleón Hernández (Associate Teacher in Physiotherapy, Universitat Internacional de Catalunya) — Principal investigator
First posted
Dec 3, 2025
Start date
Dec 2025 (estimated)
Primary completion
May 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
Dec 3, 2025

Study contacts

Daniel Pantaleon-Hernandez
Contact
daniel.pantaleon@uic.es
+34 669322784
Daniel Pantaleon-Hernandez
principal investigator · Universitat Internacional de Cataluña

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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