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Chronic Mechanical Neck PainNCT05557747

Cervicothoracic Junction Mobilization Versus Muscle Energy Technique in Chronic Neck Pain

A study testing cervicothoracic junction mobilization in form of Maitland mobilization, autogenic muscle Energy Technique and conventional physical therapy in people with Chronic Mechanical Neck Pain, run by Cairo University at 1 site in Egypt.

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

This study will be conducted to identify the difference between the effect of of cervicothoracic junction mobilization and autogenic Muscle Energy Technique. on neck pain, cervical range of motion, cervical proprioception and neck disability in mechanical neck pain patients with cervicothoracic junction hypomobility. Read more about this study

Who is it for?
Ages 18 to 45 years
Conditions the study is for
Chronic Mechanical Neck Pain
What is being tested?
cervicothoracic junction mobilization in form of Maitland mobilization, autogenic muscle Energy Technique and conventional physical therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteEgypt
Study dates
1 Nov 2022to 30 Jul 2023
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 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Patients with a primary complaint of chronic neck pain (assessed by VAS )for more than 3 months
  • Subjects with pain provocation and reduced mobility at the CT junction segment (assessed by passive accessory intervertebral movements (PAIVMs) and reduced mobility at cervical spine (assessed by CROM device.
  • patients with age range from 18 to 45 years old.
  • patients with body mass index less than 30 kg/m2.

Who cannot join

  • previous spine surgery
  • pregnancy.
  • Diabetic patients
  • Hypertensive patients
  • Patients were excluded if neck pain was associated with cervical radiculopathy
  • whiplash injuries or severe headaches
Show all 10Show fewer
  • cervical spine fracture
  • vertebro-basilar insufficiency.
  • red flags suggesting of cancer, infection, vascular insufficiency
  • Rheumatologic condition as mild systemic lupus erythematosus, poly-articular osteoarthritis, rheumatoid arthritis and advanced cervical spine degenerative diseases.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • FACULTY OF PHYSICAL THERAPY, cairo university

    Giza

Other trials in Egypt

About this study

Official title: Cervicothoracic Junction Mobilization Versus Autogenic Muscle Energy Technique in Patients With Chronic Mechanical Neck Pain

This study will be conducted to identify the difference between the effect of of cervicothoracic junction mobilization and autogenic Muscle Energy Technique. on neck pain, cervical range of motion, cervical proprioception and neck disability in mechanical neck pain patients with cervicothoracic junction hypomobility.

Being tested
cervicothoracic junction mobilization in form of Maitland mobilization, autogenic muscle Energy Technique, conventional physical therapy
Keywords
chronic mechanical neck pain, cervicothoracic junction mobilization, autogenic muscle energy technique, cervicothoracic junction hypomobility

What participants receive

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

  • cervicothoracic junction mobilization in form of Maitland mobilizationOther

    Group A: will receive cervicothoracic junction mobilization mobilization in form of Maitland mobilization to the C7-T1 level, according to their primary movement restriction (for flexion-extension restriction- central PA glide, for rotation restrictions (unilateral PA glide) for 3 sessions/week over 4 weeks periods.

  • autogenic muscle Energy TechniqueOther

    the technique will applied to neck muscles that are prone to get short including anterior, middle and posterior Scaleni, Sternocleidomastoid, Levator Scapulae and upper fibers of the Trapezius muscle.

    The AI MET group will given 3-5 repetitions of post isometric relaxation (PIR) (30-50% isometric contraction of the muscle to be stretched for 7-10 seconds, followed by rest period of 5 seconds and then a stretch of 10-60 seconds hold

  • conventional physical therapyOther

    conventional physical therapy only in form of: (superficial heat using hot pack for 10 minutes , Isometric Neck Exercises and Dynamic Neck Exercises)) for 3 sessions/week over 4 weeks periods

Study groups in NCT05557747
Study groupRoleWhat they receive
Group A:cervicothoracic junction mobilizationExperimentalGroup A: patients will receive cervicothoracic junction mobilization and conventional physical therapy program for 3 sessions/week over 4 weeks periods
Receives: Other: cervicothoracic junction mobilization in form of Maitland mobilization; Other: conventional physical therapy
Group B:autogenic muscle Energy TechniqueExperimentalGroup B: will receive autogenic muscle Energy Technique and conventional physical therapy program for 3 sessions/week over 4 weeks periods.
Receives: Other: autogenic muscle Energy Technique; Other: conventional physical therapy
Group C:conventional physical therapyActive comparatorGroup C: will receive conventional physical therapy only in form of: (superficial heat using hot pack for 10 minutes , Isometric Neck Exercises and Dynamic Neck Exercises)) for 3 sessions/week over 4 weeks periods.
Receives: Other: conventional physical therapy

What is being measured

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

  1. change in neck pain

    change in neck pain will be measured by Visual analog scale for the 3 groups pre- and post treatment

    Measured: Evaluation Will be performed prior to the first treatment session; as a baseline measure, and at last treatment session(after 4 weeks) as a post-treatment measure

Secondary outcomes (1)
  1. cervical ROM and cervical prorprioception

    cervical ROM and cervical prorprioception will be measured by cervical ROM device pre treatment and post treatment

    Measured: Evaluation Will be performed prior to the first treatment session; as a baseline measure, and at last treatment session(after 4 weeks) as a post-treatment measure

Timeline

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

  1. First posted28 Sep 2022
  2. Study start1 Nov 2022
  3. Primary completion30 Jul 2023
  4. Study completion30 Jul 2023

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
1. mobilization and conventional physical therapy 2. autogenic muscle Energy Technique and conventional physical therapy 3. conventional physical therapy only
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05557747
Sponsor's protocol ID
P.T.REC/012/003839
Status last verified
Aug 2023
First submitted
24 Sep 2022
Last updated
28 Aug 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing cervicothoracic junction mobilization in form of Maitland mobilization, autogenic muscle Energy Technique and conventional physical therapy in people with Chronic Mechanical Neck Pain, run by Cairo University at 1 site in Egypt.

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 4 inclusion and 10 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 28 Aug 2023. 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 Egypt. 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?

change in neck pain (time frame: Evaluation Will be performed prior to the first treatment session; as a baseline measure, and at last treatment session(after 4 weeks) as a post-treatment measure). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 28 Aug 2023.

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