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Upper Crossed SyndromeNCT07578831

Comparative Effects of Kendall and Feldenkrais Exercise in Upper Crossed Syndrome

A study testing Kendall Exercise Method (KM) and Feldenkrais Exercise Method (FM) in people with Upper Crossed Syndrome, run by Riphah International University at 1 site in Pakistan.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Upper Cross Syndrome (UCS) is a prevalent musculoskeletal disorder characterized by muscular imbalances and postural dysfunction. Kendall Method and Feldenkrais Method are physiotherapy exercise programs aimed at reducing pain and improving cervical position sense, CV angle and function. Read more about this study

Who is it for?
Ages 20 to 50 years
Conditions the study is for
Upper Crossed Syndrome
What is being tested?
Kendall Exercise Method (KM) and Feldenkrais Exercise Method (FM)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
72 participants
Where
1 sitePakistan
Study dates
15 Jan 2026to 15 Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 20 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Male subjects between 20-50 years
  • Female subjects between 20-50 years
  • Cranio-vertebral angle less than 50 degrees
  • Subjects who had been experiencing neck pain for more than 3 months
  • Slouched sitting for more than four hours per day
  • Usage of handheld devices while reading, working, and travelling
Show all 9Show fewer
  • Pain intensity score between 4 to 10 on NPRS
  • NDI>10 scores between 10 and 34
  • Tight pectoralis major muscle

Who cannot join

  • Surgeries of the cervical spine within past 1 year
  • Surgeries or fracture to the shoulder joint
  • Cervical instability
  • Cervical Radiculopathy
  • Neurological disorders such as cervical spondylosis, spondylolisthesis, disc prolapse and rheumatic disease

Trial locations and contacts

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

Rabiya Noor, phd contact

03344355660

Rabiya.Noor@riphah.edu.pk

Iqbal Tariq, phd contact

03338236752

Iqbal.tariq@riphah.edu.pk

Pakistan1 site, 1 recruiting
  • Rabiya Noor

    Lahore, Punjab Province, 54000

    iqbal Tariq, 03338236752, iqbal.tariq@riphah.edu.pk

    Recruiting

Other trials in Pakistan

About this study

Official title: Comparative Effects of Kendall and Feldenkrais Exercise on Pain, Cervical Position Sense, Craniovertebral Angle and Function in Upper Crossed Syndrome

Upper Cross Syndrome (UCS) is a prevalent musculoskeletal disorder characterized by muscular imbalances and postural dysfunction. Kendall Method and Feldenkrais Method are physiotherapy exercise programs aimed at reducing pain and improving cervical position sense, CV angle and function. This study compares their effects on pain, CV angle, cervical position sense, and disability in individuals with upper cross syndrome. This will be a randomized Controlled trial conducted on 72 participants. Data will be collected from Sikander Medical Complex, Gujranwala by using non-probability convenience sampling technique. Adults aged 20 to 50 years with upper cross syndrome, confirmed by Craniovertebral Angle less than 50 degrees and experiencing symptoms for more than four weeks, will be included in this study. Individuals with cervical spondylosis, spondylolisthesis, disc prolapse, trauma-related cervical injuries, or a history of shoulder surgery will be excluded. Group A will receive Kendall Method along with conservative physiotherapy, while Group B will receive Feldenkrais Method combined with conservative physiotherapy. Each session will last 30 minutes-40 minutes for the primary intervention and 15-20 minutes for conventional therapy-administered three times per week for five weeks. Pre- and post-treatment evaluations will include the Numeric Pain Rating Scale (NPRS), CV angle (measured via Image J), Cervical position Sense (assessed via HRE) and functional disability (measured via NDI). Data will be analyzed using SPSS version 27.0.

Being tested
Kendall Exercise Method (KM), Feldenkrais Exercise Method (FM)
Keywords
Postural Disorders, Neck pain, Muscle weakness
Medical subject headings
Oculocerebral hypopigmentation syndrome type Preus, Neck Pain, Muscle Weakness

What participants receive

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

  • Kendall Exercise Method (KM)Other

    Strengthening of deep cervical flexors Procedure: Positioning supine with the chin tucked in and lifting the head for 2 to 8 s. Stretching of cervical extensors Procedure: Maintaining a sitting posture, with hands on the occipital region, and flexed spine while moving head downwards to stretch cervical extensors. Strengthening of retractors Procedure: Maintaining an upright posture, keep the resistance band circling with strong support and stretching it with the upper limbs of both sides so that there is full retraction of the scapula

  • Feldenkrais Exercise Method (FM)Other

    Shoulder 1 minute (2) Relaxation (2) Lift and lower one shoulder slowly Key Focus Focus on small range of motion and awareness Neck Rolls head from one side to the other gently 1 minute Reduce tension, no strain, smooth motion Ear-to-Shoulder (Static) Lower ear to shoulder, return to center 1 minute Observe full-body involvement Ear-to-Shoulder with Shoulder Lift Alternate ear-to-shoulder and shoulder-to-ear 1 minute Gentle coordination of ]head and shoulder Upper Body Rotation (Step 1) Sit forward on chair; rotate upper body right slightly 6-10 Reps Relaxed turning, observe visual range Eyes Fixed with Body Rotation Fix eyes forward, turn upper body right 6-10 Reps Notice effect of eye fixation on motion

Study groups in NCT07578831
Study groupRoleWhat they receive
Kendall Exercise Method (KM)ExperimentalNot described
Receives: Other: Kendall Exercise Method (KM)
Feldenkrais Exercise Method (FM)Active comparatorNot described
Receives: Other: Feldenkrais Exercise Method (FM)

What is being measured

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

  1. Neck pain and diability index

    The NDI is used to measure functional impairment and pain because to its high reliability and validity. A higher NDI score indicates a more severe impairment; the ten parts of the NDI are rated from zero to fifty. With a maximum score of 50, each item may be assessed on a scale from 0 (no disability) to 5 (total impairment). The maximum possible score for each part is 5.

    If the first statement is marked as true, the section score is 0, and if the final statement is recorded as true, the score is 5. No neck impairment is considered to exist with a score of 0 4, mild disability from 5-14, moderate disability from 15-24, severe disability from 25-34, and full disability from scores over 34(11). The Neck Disability Index exhibited excellent reliability (ICC = 0.92; [95 % CI: 0.46-0.97]).(27)

    Measured: 6th week

  2. Head Repositioning Error Test

    The Arc tangent of the distance between the reference and target points divided by the distance between reference point and the laser pointer was considered as HRE.This method was first described by Revel et al. Each participant performed three trials. The average amount of three HRE was used for data analysis. No discomfort or complication was reported by participants after HRE test. The CVA and HRE were measured by two different physiotherapists.(29)

    Measured: 6th week

Timeline

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

  1. First posted11 May 2026
  2. Study start15 Jan 2026
  3. Primary completion15 May 2026 (estimated)
  4. Study completion15 Jun 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
Masking
Single blind
Who is masked
Participant
Enrolment
72 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07578831
Sponsor's protocol ID
REC/RCR & AHS/25/0108
Status last verified
May 2026
First submitted
5 May 2026
Last updated
11 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Kendall Exercise Method (KM) and Feldenkrais Exercise Method (FM) in people with Upper Crossed Syndrome, run by Riphah International University at 1 site in Pakistan.

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 9 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 11 May 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 Pakistan. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Rabiya Noor, phd (03344355660, Rabiya.Noor@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Neck pain and diability index (time frame: 6th week). The study lists 2 primary outcomes in all. 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 11 May 2026.

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