Can a simple manual therapy reshape the hump and ease neck pain?

NCT ID NCT07705841

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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By invitation only
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The trial has finished. Results may not be published yet.
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Cancelled before anyone took part.

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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

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First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time

Summary

This study investigates whether the Mulligan technique, a hands-on therapy using gentle gliding movements on the spine, can improve posture, reduce pain, and increase neck and back mobility in women aged 39 to 58 with Dowager's hump (forward head posture). Participants will receive either the Mulligan technique plus standard exercises or standard exercises alone. The main outcomes measured are changes in the craniovertebral angle (a measure of head posture) and pain intensity.

What this could mean

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

Active substance
Mulligan technique (a manual therapy involving sustained natural apophyseal glides for the neck and upper back)
What this could lead to
If effective, this approach could offer a non-invasive way to improve posture, reduce pain, and increase neck and back mobility in women with Dowager's hump.
What could go wrong
This is a small, early-stage study with 56 participants, so results may not apply to everyone. The technique requires a skilled therapist, and benefits may vary.

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 56 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Feb 2027

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

39 to 58 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: * The age of patients will be ranged from 39 to 58 years old; mean menopausal age * The patients with CVA were less than 50°. * Pain intensity level will be examined by VAS which will be more than 3. * Limited cervical range of motion . * Limited thoracic range of motion (flexion, extension) * BMI will be more than 30 kg \\m2. Exclusion Criteria: * Patients with any neck surgeries. * Neurological infection and spinal cord injury. * Patients with congenital musculoskeletal deformities or ankylosing spondylitis. * Patients with cervical trauma or car accident.

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