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Posture training promises triple relief for overburdened housewives

NCT ID NCT07203950

Symptom relief Sponsor: Riphah International University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a gentle exercise method called global postural reeducation in 30 housewives aged 25-40 who have had low back pain for over 3 months. The goal is to see if it can reduce pain, lower stress, and improve sleep quality. Unlike painkillers, this approach focuses on retraining the body's posture and movement patterns to address both physical and mental strain.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2025

An estimate. Start dates often move.

Expected to finish

Apr 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

25 to 40 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Participants' full filling the criteria given below will be recruited in this study. Diagnosis based on clinical guidelines linked to the International Classification of Function, Disability and Health of the Orthopedic Section of the American Physiotherapy Association. 1. Housewives (Age 25-40 years) 2. Chronic nonspecific LBP (more than 3 months) 3. Experience mild to moderate stress (measured by perceived stress scale) 4. Sleep disturbances or poor sleep quality (PSQI score\>5) Exclusion Criteria: Participant falling in this category would be excluded of the study. 1. Pregnancy. 2. Using NSAIDs. 3. Acute, subacute LBP. 4. Females having diagnosed irregular/prolonged menstrual cycles. 5. History of recent Spinal surgery (within the past year). 6. Neurological deficits (foot drop, motor weakness). 7. Diagnosed severe psychiatric issues (e.g. severe depression, bipolar disorder, psychosis). 8. Use of sleep medications, antidepressants, or anxiolytics during the study period. 9. Specific causes of LBP (herniated disc, lumbar stenosis, spinal deformity, fracture, spondolysthesis). 10. Systemic diseases (tumor, Rhematoid arthritis)

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Conditions

The condition(s) this trial relates to.

insomnia Low Back Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Low back pain Sleep quality Stress

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Dr Zushmaleen Ahmed Chughtai Physiotherapy Clinic

    Kot Addu, Punjab Province, Pakistan

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