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Comparative Effects of Egoscue and Feldenkrais Exercises on in Upper Cross Syndrome

Comparative Effects of Egoscue and Feldenkrais Exercises on Pain, Craniovertebral Angle and Functional Disability in Upper Cross Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07628413
Enrollment
48
Registered
2026-06-05
Start date
2025-12-15
Completion date
2026-07-15
Last updated
2026-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Upper Cross Syndrome

Keywords

Craniovertebral angle,, upper cross syndrome

Brief summary

Upper cross syndrome is a common postural dysfunction that is caused due to alternating tightness and weakness in the opposite muscle groups of the neck, shoulders and upper back which results in abnormal postural deviations. The aim of the study will be to compare the effects of Egoscue exercises and Feldenkrais exercises on pain, craniovertebral angle and functional disability in upper cross syndrome. A Randomized clinical trial will be conducted at Ghurki Trust Teaching Hospital, Lahore and Riphah clinic, Lahore through non probability convenience sampling technique on 54 patients which will be allocated using simple random sampling through sealed opaque envelop into Group A and Group B. Group A will be treated with Egoscue exercises and conventional therapy and Group B will be treated with Feldenkrais exercises and conventional therapy at the frequency of 3 sets with 10 repetitions thrice a week. Outcome measures will be conducted through pain, craniovertebral angle and functional disability after 4 weeks. Data will be analyzed with SPSS software version 26. After assessing the normality of data by Shapiro-Wilk test, it will be decided either parametric or non- parametric will be used within the group or between the groups.

Interventions

* Static Back (for 5 - 10 minutes) * Cervical retractions (10- 15 reps) * Wall Angels (2 sets of 10) * Standing arm circles (40 forward reps \& 40 backward reps) * Static wall (for 5-8 minutes) * Modified pre stretch on wall (Hold for 30- 45 secs on each side) * Air bench (for 1- 2 minutes) * Tower shoulder rolls (stay for 10 minutes)

* Shoulder Circles with awareness * Head Rolls with Breath awareness * Arm Clock (Arm circles on the floor) * Scapular Glides * Pelvic clock with shoulder integration * Shoulder blades and arm lifting

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 25 to 45 years * Both genders (male and female) * Chronic neck pain for more than three months - NPRS (3 to 7) * Craniovertebral angle less than 50 degrees * Tight Pectoralis muscle and trapezius * Weak rhomboids and deep neck flexors

Exclusion criteria

* Any malignancy related to soft tissue and shoulder joint * Congenital joint deformity * Recent fractures to joint * Recent surgery of shoulder joint or associated structures * Patients with shoulder dislocation

Design outcomes

Primary

MeasureTime frameDescription
Disability Index (DNI)6th weekThis questionnaire will be used to asses disability. It comprises of 10 items; 7 related to daily living activities; 2 related to pain and 1 related to concentration. Each item is scored from 0 to 5. Total score is expressed as a percentage, with higher scores related to greater disability. Minimum detectable change measurements vary from 4.2 to 13.4, and minimum clinically important differences vary from 5 and 9.5
Craniovertebral angle (CVA)6th weekCraniovertebral angle can be measured with Image J software. If the angle is less than 50 degrees (\< 50 degree). The angle will be between tragus of the ear to cervical spinous process C7.

Countries

Pakistan

Contacts

CONTACTRabiya Noor, phd
Rabiya.Noor@riphah.edu.pk03344355660
CONTACTIqbal Tariq, phd
Iqbal.tariq@riphah.edu.pk03338236752
PRINCIPAL_INVESTIGATORareesha shakeel, MSPT(CP)

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 6, 2026