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Recruiting NCT07576296

NCT07576296 Effects of Scapular Posterior Tilt Exercises and Cross-Body Stretching in Postpartum Women With Rounded Shoulders

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Clinical Trial Summary
NCT ID NCT07576296
Status Recruiting
Phase
Sponsor Riphah International University
Condition Postpartum Complication
Study Type INTERVENTIONAL
Enrollment 34 participants
Start Date 2025-10-01
Primary Completion 2026-06-01

Eligibility & Interventions

Sex Female only
Min Age 20 Years
Max Age 35 Years
Study Type INTERVENTIONAL
Interventions
Scapular Posterior Tilt exercisesCross-Body Stretching

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 34 participants in total. It began in 2025-10-01 with a primary completion date of 2026-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to compare the effects of scapular posterior tilt exercises and cross-body stretching on breastfeeding efficiency, latch quality, and posture in postpartum women with rounded shoulders.

Eligibility Criteria

Inclusion Criteria: * Mutiparous females. * previous cesarean section deliveries * Postpartum women between 2 weeks and 6 months postpartum. * Experiencing shoulder discomfort or poor posture Exclusion Criteria: * History of recent trauma or surgery such a Arthroscopy for Impingement Syndrome, Shoulder Replacement that affecting the shoulder complex. * Mother with history of breast cancer and hepatitis * History of shoulder surgery, trauma, or musculoskeletal disorders affecting the upper back/shoulder (Trapezius muscles train, Levator scapulae and rhomboid overuse) * Severe postnatal complications (e.g., mastitis, postpartum depression, uncontrolled hypertension or diabetes.

Contact & Investigator

Central Contact

imran amjad

✉ imran.amjad@riphah.edu.pk

📞 03324390125

Principal Investigator

hina gul, PhD*

PRINCIPAL INVESTIGATOR

Riphah International University

Frequently Asked Questions

Who can join the NCT07576296 clinical trial?

This trial is open to female participants only, aged 20 Years or older, up to 35 Years, studying Postpartum Complication. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07576296 currently recruiting?

Yes, NCT07576296 is actively recruiting participants. Contact the research team at imran.amjad@riphah.edu.pk for enrollment information.

Where is the NCT07576296 trial being conducted?

This trial is being conducted at Lahore, Pakistan.

Who is sponsoring the NCT07576296 clinical trial?

NCT07576296 is sponsored by Riphah International University. The principal investigator is hina gul, PhD* at Riphah International University. The trial plans to enroll 34 participants.

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