Effects of Global Postural Reeducation on Psychophysical Wellbeing in Housewives With Chronic Non… (NCT07203950) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effects of Global Postural Reeducation on Psychophysical Wellbeing in Housewives With Chronic Non-specific LBP.
Pakistan30 participantsStarted 2025-09-30
Plain-language summary
This study aims to explore the multidimensional impact of Global postural reeducation in a population that is not only physically overburdened but also psychologically strained due to the demands of domestic life. Unlike conventional therapies that often focus solely on pain relief, GPR offers a comprehensive intervention model that may simultaneously enhance physical function, reduce psychological stress, and improve sleep quality. By targeting housewives with chronic non-specific LBP, this study seeks to fill a critical gap in the literature and provide evidence for a more inclusive, preventive, and non-pharmacological approach to musculoskeletal and mental health management
Who can participate
Age range
25 Years – 40 Years
Sex
FEMALE
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
. Housewives (Age 25-40 years)
. Chronic nonspecific LBP (more than 3 months)
. Experience mild to moderate stress (measured by perceived stress scale)
. Sleep disturbances or poor sleep quality (PSQI score\>5)
Exclusion criteria
. Pregnancy.
. Using NSAIDs.
. Acute, subacute LBP.
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
1
numeric pain rating scale
Timeframe: Assessed at Baseline, 3 weeks, and 6-week follow-up.
2
lumber ROMs using inclinometer
Timeframe: Assessed at Baseline, 3 weeks, and 6-week follow-up.
3
perceived stress scale
Timeframe: Assessed at Baseline, 3 weeks, and 6-week follow-up.
4
Pittsburg sleep quality index
Timeframe: Assessed at Baseline, 3 weeks, and 6-week follow-up.