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Cervical DiseaseNCT07324811

Effectiveness of a Home-based Cervical Motor Control Exercise Programme Versus Conventional Manual Therapy in Patients With Post-whiplash Neck Pain.

A study testing conventional physiotherapy treatment in people with Cervical Disease, run by Universidad Pontificia de Salamanca at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Whiplash-associated disorders are a common cause of persistent neck pain following traffic accidents and are frequently associated with impairments in cervical motor control, pain, and functional disability. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Cervical Disease
What is being tested?
conventional physiotherapy treatment
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteSpain
Study dates
10 Jan 2025to 10 Sep 2025
Phase
Interventional
Are there results?
None posted in the registry

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

  • Patients who met the following criteria were included:
  • Age between 18 and 65 years.
  • Clinical diagnosis of post-whiplash neck pain resulting from a traffic accident.
  • Symptoms lasting longer than four weeks.
  • Presence of neck pain with a minimum intensity of 3 points on the Visual Analogue Scale.
  • Ability to understand and follow the instructions of the home exercise programme.
  • Signed informed consent.

Who cannot join

  • Patients with the following conditions were excluded:
  • Signs of severe neurological compromise or significant structural cervical pathology (fractures, cervical instability, myelopathy).
  • History of cervical surgery.
  • Rheumatic, neurological, or systemic diseases that could influence the results.
  • Previous physiotherapy treatment for the same episode in the three months prior to the study.
  • Pregnancy or any medical contraindication for therapeutic exercise.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Universidad Pontificia de Salamanca

    Salamanca, 37002

Other trials in Spain

About this study

Official title: Effectiveness of a Home-based Cervical Motor Control Exercise Programme Versus Conventional Manual Therapy in Patients With Post-whiplash Neck Pain: a Randomised Clinical Trial.

Whiplash-associated disorders are a common cause of persistent neck pain following traffic accidents and are frequently associated with impairments in cervical motor control, pain, and functional disability. Therapeutic exercise aimed at restoring cervical motor control has shown promising results; however, evidence regarding the effectiveness of structured home-based exercise programs compared with conventional physiotherapy remains limited. The aim of this study was to compare the effectiveness of a home-based cervical motor control exercise program versus conventional physiotherapy in patients with whiplash-associated neck pain.

A randomized controlled trial with two parallel groups was conducted. Patients diagnosed with whiplash-associated neck pain were randomly assigned to either an experimental group performing a structured home-based cervical motor control exercise program or a control group receiving conventional physiotherapy based on manual therapy and cervical mobilization techniques. Outcome measures included pain intensity assessed using the Visual Analogue Scale, functional disability measured with the Neck Disability Index, and active cervical range of motion. Assessments were performed at baseline and after an eight-week intervention period.

Being tested
home-based cervical motor control exercise programme, conventional physiotherapy treatment
Keywords
Whiplash, pain, exercise
Medical subject headings
Uterine Cervical Diseases, Whiplash Injuries, Pain, Motor Activity

What participants receive

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

  • home-based cervical motor control exercise programmeProcedure or surgery

    home-based programme of active cervical motor control exercises supervised by physiotherapists

  • conventional physiotherapy treatmentProcedure or surgery

    Conventional physiotherapy treatment with passive therapy (manual therapy) carried out in a physiotherapy clinic.

Study groups in NCT07324811
Study groupRoleWhat they receive
home-based cervical motor control exercise programmeExperimentalhome-based cervical motor control exercise programme monitored by physiotherapists
Receives: Procedure: home-based cervical motor control exercise programme
conventional physiotherapy treatmentActive comparatorConventional physiotherapy treatment including passive therapies (manual therapy) in the physiotherapy clinic.
Receives: Procedure: conventional physiotherapy treatment

What is being measured

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

  1. pain

    measured using the visual analogue pain scale (VAS) (where 0 is the least possible pain and 10 is the maximum possible pain)

    Measured: 2 months

Secondary outcomes (1)
  1. range of motion

    The range of active cervical movement was assessed using goniometry, recording the movements of flexion, extension, rotation, and lateralisation of the cervical spine.

    Measured: 2 months

Timeline

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

  1. First posted8 Jan 2026
  2. Study start10 Jan 2025
  3. Primary completion10 Apr 2025
  4. Study completion10 Sep 2025

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
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
80 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07324811
Sponsor's protocol ID
00043
Status last verified
Dec 2025
First submitted
23 Dec 2025
Last updated
8 Jan 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Randlov A, Ostergaard M, Manniche C, Kryger P, Jordan A, Heegaard S, Holm B. Intensive dynamic training for females with chronic neck/shoulder pain. A randomized controlled trial. Clin Rehabil. 1998 Jun;12(3):200-10. doi: 10.1191/026921598666881319.

    PubMed 9688035
  • Jordan A, Bendix T, Nielsen H, Hansen FR, Host D, Winkel A. Intensive training, physiotherapy, or manipulation for patients with chronic neck pain. A prospective, single-blinded, randomized clinical trial. Spine (Phila Pa 1976). 1998 Feb 1;23(3):311-8; discussion 319. doi: 10.1097/00007632-199802010-00005.

    PubMed 9507618
  • Bronfort G, Evans R, Nelson B, Aker PD, Goldsmith CH, Vernon H. A randomized clinical trial of exercise and spinal manipulation for patients with chronic neck pain. Spine (Phila Pa 1976). 2001 Apr 1;26(7):788-97; discussion 798-9. doi: 10.1097/00007632-200104010-00020.

    PubMed 11295901
  • Kjellman GV, Skargren EI, Oberg BE. A critical analysis of randomised clinical trials on neck pain and treatment efficacy. A review of the literature. Scand J Rehabil Med. 1999 Sep;31(3):139-52. doi: 10.1080/003655099444489.

    PubMed 10458312

Questions about this trial

What is this clinical trial studying?

A study testing conventional physiotherapy treatment in people with Cervical Disease, run by Universidad Pontificia de Salamanca at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

pain (time frame: 2 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07324811, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jan 2026.

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