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Chronic Neck PainNCT07260955

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

A study testing Thoracic exercise program and education and Thoracic and neck specific exercise program and education in people with Chronic Neck Pain and Non-specific Neck Pain, run by Universitat Internacional de Catalunya at 1 site in Spain.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial 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… Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Chronic Neck Pain, Non-specific Neck Pain
What is being tested?
Thoracic exercise program and education and Thoracic and neck specific exercise program and education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 siteSpain
Study dates
Dec 2025to Jun 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Daniel Pantaleon-Hernandez contact

+34 669322784

daniel.pantaleon@uic.es

Spain1 site
  • Universitat Internacional de Cataluña

    Sant Cugat del Vallès

    Universitat Internacional de Cataluña, 935042000, nnogales@uic.es

Other trials in Spain

About this study

Official title: Effects of a Multimodal Telerehabilitation Program in Patients With Chronic Non-Specific Neck Pain: Randomized Clinical Trial.

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.

Being tested
Thoracic exercise program and education, Thoracic and neck specific exercise program and education
Keywords
Neck muscles, Chronic neck pain, Telerehabilitation, Exercise therapy, Pain education

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Thoracic exercise program and educationOther

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

  • Thoracic and neck specific exercise program and educationOther

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

Study groups in NCT07260955
Study groupRoleWhat they receive
Experimental groupExperimentalThoracic spine mobility, deep cervical flexor and extensor muscles strength training, thoracic muscles strength training and pain education through telerehabilitation.
Receives: Other: Thoracic and neck specific exercise program and education
Control groupActive comparatorThoracic spine mobility, thoracic muscles strength training and pain education through telerehabilitation.
Receives: Other: Thoracic exercise program and education

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain intensity

    Measured by Visual Analogue Scale.

    Measured: Baseline, 6 weeks, 1 month follow-up

  2. Neck Disability

    Measured by the Spanish version of Neck Disability Index Questionnaire.

    Measured: Baseline, 6 weeks, 1 month follow-up

Secondary outcomes (5)
  1. Activation of deep neck flexors muscles.

    Measured by Cranio-cervical flexion test

    Measured: Baseline, 6 weeks, 1 month follow-up

  2. Forward head posture

    Measured by craniovertebral angle.

    Measured: 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.

    Measured: Baseline, 6 weeks, 1 month follow-up

  4. Kinesiophobia

    Measured with Spanish version of Tampa Scale

    Measured: Baseline, 6 weeks, 1 month follow-up

  5. Global Rating of Change

    Measured by Global Rating of Change Scale

    Measured: 1 month follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Dec 2025
  2. Study startDec 2025 (estimated)
  3. Primary completionMay 2026 (estimated)
  4. Study completionJun 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This will be a randomized controlled trial with 2 different groups.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
54 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07260955
Sponsor's protocol ID
FIS-2024-009
Status last verified
Nov 2025
First submitted
21 Nov 2025
Last updated
3 Dec 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

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