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Tape or cups? new study tests two simple therapies for hunchback pain

NCT ID NCT07373925

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two non-invasive treatments—kinesio taping and dry cupping—for people with thoracic kyphosis (an excessive rounding of the upper back). Researchers will measure changes in pain and the angle of the curve in 48 physically active adults aged 18 to 30. The goal is to see which therapy works better for easing discomfort and improving posture.

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 48 people

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

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Jun 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 30 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: * Subjects with thoracic kyphosis angle \> 40° diagnosed by a medical doctor will be selected from Damietta University's clinic of physical education faculty. * Subjects from both genders with an age range between 18 and 30 years . * Subjects who are physically active in physical education sessions Exclusion Criteria: * Subjects with medical conditions that restrict activity. * Those who received exercise intervention for kyphosis. * Structural thoracic kyphosis, defined as thoracic kyphosis that did not partially or completely disappear during prone extension, as assessed by a physical therapist. * Medical history of spinal fracture, spinal surgery, shoulder joint injury or pelvic injury. * Other spinal diseases; presence of scoliosis on Adam's forward bend test. * Spinal kyphosis due to visible thoracic deformity. * Subjects undergoing professional sports training. * Skin disease (dermatitis, psoriasis), neurological disease or cancer. * Using anticoagulants or nonsteroidal antidepressants. * Inflammatory or rheumatologic disorders of the spine. * Severe cardiopulmonary disease, rheumatic disease or pregnancy. * Have a pacemaker or metal implants. * Do not understand the written consent form.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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  1. The official record

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More trials for these conditions

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