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Recruiting NCT07593183

NCT07593183 Comparing the Effects of Lumbar Stability Exercises and Telerehabilitation on Reducing Lumbar Lordotic Angle, Pain, and Disability in Postpartum Women

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Clinical Trial Summary
NCT ID NCT07593183
Status Recruiting
Phase
Sponsor Foundation University Islamabad
Condition Lumbar Lordotic Angle
Study Type INTERVENTIONAL
Enrollment 38 participants
Start Date 2026-05-13
Primary Completion 2026-07-01

Eligibility & Interventions

Sex Female only
Min Age 20 Years
Max Age 40 Years
Study Type INTERVENTIONAL
Interventions
Lumbar stabilizationTelerehabilitation

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 38 participants in total. It began in 2026-05-13 with a primary completion date of 2026-07-01.

⚠ 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

Low back pain is the most common symptoms experienced by people throughout the world. Although lifetime prevalence of low back pain among women is more but it is particularly common during pregnancy, affecting approximately 50% of women. Pregnancy induces significant physiological changes, which lead to increased ligamentous laxity that may persist for 3 to 6 months postpartum. Additionally, the expanding uterus shifts the maternal center of gravity anteriorly, resulting in compensatory lumbar hyperlordosis and contributing to lower back discomfort. While these adaptations help accommodate pregnancy, they often do not fully resolve after birth, especially in the presence of abdominal muscle weakness. The result is altered posture characterized by an exaggerated lumbar lordotic curve that may predispose postpartum women to continued pain and lumbar instability. Without a structured postpartum rehabilitation program, these postural abnormalities may go uncorrected. Ensuring adherence and completion of such programs is critical for preventing long-term musculoskeletal complication. There are many efficient way to help in maintaining adherence and completion of program including the use of digital platforms. The increasing availability of low cost internet and communication technologies has enhanced the capacity to deliver healthcare services through internet, enabling broader access to physiotherapy services and follow-up care through telerehabilitation. Telerehabilitation is one of the emerging field of telemedicine, defined as set of tools, procedure, and protocols to deliver the rehabilitation process remotely. The objective of the study is to facilitate implementation of the telerehabilitation for home based program for postpartum female. The objectives of the study is to compare the effectiveness of telerehabilitation-based lumbar stability exercises versus on-site lumbar stability exercises in improving lumbar stability among postpartum female and to facilitate implementation of the telerehabilitation for home based program for postpartum female. It is a randomized controlled trial. Participants meeting the inclusion criteria will be recruited and consent form will be taken than participants will be allocated to group A (On-Site Lumbar Stability exercise) and B (Telerehabilitation) through 1:1 method. Pre-treatment assessment will be carried out on Day 1 using the outcome measures tool like NPRS, ODI and LLA. Participant will receive intervention for 6 weeks, 3 sessions per weeks. After the completion, on 6 week Post-treatment assessment will be carried out using the same outcome measures tool like NPRS, ODI and LLA.

Eligibility Criteria

Inclusion Criteria: * Female participants 6 weeks up to 12 month post-partum women. * Participants who has access to internet services and technologies * Participants with mild-to-moderate self-reported low back pain for at least 2 weeks. * Objectively measured lumbar lordotic angle beyond normative range of 40 Degree Exclusion Criteria: * Congenital spine deformities like scoliosis * Pelvic prolapsed

Contact & Investigator

Central Contact

Ayesha Khan, DPT

✉ Ayeshakh877@gmail.com

📞 03025220691

Principal Investigator

Ayesha Khan, DPT

PRINCIPAL INVESTIGATOR

Foundation University Islamabad

Frequently Asked Questions

Who can join the NCT07593183 clinical trial?

This trial is open to female participants only, aged 20 Years or older, up to 40 Years, studying Lumbar Lordotic Angle. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07593183 currently recruiting?

Yes, NCT07593183 is actively recruiting participants. Contact the research team at Ayeshakh877@gmail.com for enrollment information.

Where is the NCT07593183 trial being conducted?

This trial is being conducted at Islamabad, Pakistan.

Who is sponsoring the NCT07593183 clinical trial?

NCT07593183 is sponsored by Foundation University Islamabad. The principal investigator is Ayesha Khan, DPT at Foundation University Islamabad. The trial plans to enroll 38 participants.

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