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Gentle touch for back pain: 6-Week therapy trial aims to loosen stiff tissues

NCT ID NCT07667062

Symptom relief Sponsor: University of Health Sciences Lahore 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a 6-week program of myofascial release—a manual therapy using sustained gentle pressure on the lower back—can reduce pain and improve movement in adults with chronic non-specific low back pain. 65 participants will receive either the real therapy or a sham version. Researchers will measure changes in tissue stiffness, pain confidence, and daily function.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
myofascial release therapy (manual pressure technique)
What this could lead to
If it works, this could provide a non-drug, hands-on therapy option to ease chronic low back pain and improve daily function.
What could go wrong
This is a small, early-stage trial with only 65 people. The sham group may also improve, and long-term benefits are unknown. Results may not apply to everyone with back pain.

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 65 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Aug 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

18 to 60 years

Sex

Anyone

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: * Adults aged 18-60 years * Non-specific low back pain duration \> 12 weeks * Average pain intensity NRS ≥ 3 over the past week * Able to provide written informed consent * Able to attend 18 supervised sessions over 6 weeks (3 sessions/week) Exclusion Criteria: * Specific spinal pathology (fracture, disc herniation with neurological deficit, spinal stenosis, inflammatory arthropathy, malignancy) * Previous lumbar surgery * Current pregnancy * Severe psychiatric disorder or active psychosis * Manual therapy or physiotherapy for LBP within the previous 3 months * Systemic connective tissue disorder (e.g., Ehlers-Danlos syndrome, Marfan syndrome) * Contraindication to ultrasound imaging or manual therapy.

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As listed by the trial registrant

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

Chronic non specific low back pain

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

  • Affiliated Teaching Hospitals of University of Health Sciences Lahore

    Lahore, Punjab Province, Pakistan

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