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New exercise combo shows promise for shoulder pain relief

NCT ID NCT07521839

Symptom relief Sponsor: Superior University Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether adding a specific breathing technique (abdominal drawing-in) and cross-pattern limb exercises to standard physical therapy can reduce pain and improve movement in people with shoulder impingement syndrome. 38 adults aged 30-50 with shoulder pain will be split into two groups: one gets standard care, the other adds the new exercises. The goal is to see if the new approach leads to better pain relief and shoulder function after 4 weeks.

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

38 people

The number who actually took part.

Started

Feb 2026

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

30 to 50 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: 1. Patients with age group 30-50 2. Both male and females 3. Positive Neer's sign, positive Hawkins Kennedy sign, , 4. Pain with positive painful arc. Pain with resisted isometric abduction Exclusion Criteria: 1. History of shoulder dislocation 2. Patients underwent any shoulder joint surgery. 3. Fracture of upper limb. 4. Patient who has current symptoms related to the cervical spine, 5. Patient who has a history of acromioclavicular pain 6. Patient having history low back pain 7Corticosteroid injection into the shoulder joint in the previous 12 months

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Conditions

The condition(s) this trial relates to.

shoulder impingement syndrome Shoulder Pain

As listed by the trial registrant

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

Shoulder impingement syndrome

Contacts and locations

Locations

  • Suyperior Univeristy

    Lahore, Punjab Province, 53720, Pakistan

More trials for these conditions

Other studies related to the condition(s) this trial covers.