RecruitingNot Applicable

Pelvic Control Training Using Pressure Biofeedback Versus Core Stability Training in Non-Specific Low Back Pain

Pakistan50 participantsStarted 2026-07-16

Plain-language summary

To compare the effects of pelvic control training using pressure biofeedback with core stability training on pain, range of motion, muscle strength, and functional disability in patients with non specific low back pain

Who can participate

Age range

18 Years – 30 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Children aged 18-30 years. * The body mass index within the typical range of 18.5 to 24.9 kg/m². * No history of musculoskeletal, neurological, or vestibular disorders. * Physically active individuals not engaged in regular core or balance training programs in the last 3 months. * Willing to provide informed consent and comply with the study protocol. Exclusion Criteria: * History of lower extremity, spinal, or pelvic injuries in the past 6 months. * Current pain, dizziness, or balance impairments. * Known postural deformities (e.g., scoliosis, hyper lordosis). * Neurological, cardiovascular, or systemic conditions affecting balance or motor performance. * Pregnancy or recent childbirth (\<6 months) * Participation in any other interventional study during the study period.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Oswestry Disability Index (ODI)

Timeframe: 6 weeks

Numeric Pain Rating Scale (NPRS)

Timeframe: 6 weeks

Bubble Inclinometer

Timeframe: 6 weeks

Pressure Biofeedback Unit (PBU)

Timeframe: 6 weeks

Trial details

NCT IDNCT07726797

SponsorRiphah International University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-08-25

Contact for this trial

Imran Amjad, PhD

03324390125 imran.amjad@riphah.edu.pk

View on ClinicalTrials.gov More Non Specific Low Back Pain trials

Who can participate

Age range

18 Years – 30 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.