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Shoulder Impingement SyndromeNCT07237789

Impact of Core Stability Training on Pain and Function in Patient With Shoulder Impingement Syndrome Among Manual Operated Hand Workers

A study testing Experimental in people with Shoulder Impingement Syndrome, run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Even at the early stage of employment exposure to mechanical factors such as lifting heavy weights, working with hands at or above shoulder level, and pushing or pulling heavy loads are independent risk factors for new-onset shoulder pain . Read more about this study

Who is it for?
Ages 25 to 40 years
Conditions the study is for
Shoulder Impingement Syndrome
What is being tested?
Experimental
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
No sites listed yet
Study dates
Aug 2026to Sep 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • manually operated hand workers (males and females), Age from 25-to
  • -40 years, Shoulder impingement syndrome, and with No previous history of shoulder surgery that may affect their performance.

Who cannot join

  • Patient who has a history of shoulder instability, History of shoulder dislocation, Patient who has current symptoms related to the cervical spine, Patient who has a history of acromioclavicular pain, and Low back pain (LBP) will be excluded.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Salah Eid Ahmed Ali contact

+01158125773

Salah.Eid@Sue.edu.eg

About this study

Even at the early stage of employment exposure to mechanical factors such as lifting heavy weights, working with hands at or above shoulder level, and pushing or pulling heavy loads are independent risk factors for new-onset shoulder pain . Shoulder-related problems among workers doing spading are 53.1% and 57.7% among workers brick carrying tasks, these shoulder issues may be the result of repetitive awkward movement (beyond ninety degree raising with abduction position) of the shoulder during these activities .

Read the detailed description

The highest prevalence of shoulder impingement syndrome is among slaughterhouses as they are exposed to a combination of repetitive shoulder movements and sustained elevated arm .

Several of workplace physical exposures are implicated in the causation and/or increasing shoulder disorders. Occupational exposures including manual handling heavy lifting, pushing, pulling, holding, carrying), working above shoulder height, and repetitive work are the most frequent causes of shoulder disorders specifically the subacromial impingement syndrome.

Shoulder-related problems among workers doing spading are 53.1% and 57.7% among workers brick carrying tasks, these shoulder issues may be the result of repetitive awkward movement (beyond ninety degree raising with abduction position) of the shoulder during these activities.

Being tested
Experimental, Control
Keywords
Core Stability, Function, Hand Worker, Shoulder Impingement
Medical subject headings
Shoulder Impingement Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ExperimentalOther

    Core stability training will be used for experimental group

  • ControlOther

    Traditional physiotherapy

Study groups in NCT07237789
Study groupRoleWhat they receive
ControlActive comparatorControl group will receive traditional physiotherapy
Receives: Other: Control
ExperimentalExperimentalNot described
Receives: Other: Experimental

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain intensity level

    Numerical Pain Rating Scale will be used to assess shoulder pain intensity level with zero indicates there is no pain and ten indicates the pain is severe intolerable

    Measured: 8 weeks

Secondary outcomes (1)
  1. Function

    DASH-Arabic a self-administered outcome measure will be used to assess disability in patients

    Measured: 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Nov 2025
  2. Study startAug 2026 (estimated)
  3. Primary completionSep 2026 (estimated)
  4. Study completionSep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07237789
Sponsor's protocol ID
SREC.PT.SUE(17)925
Status last verified
Aug 2026
First submitted
1 Oct 2025
Last updated
28 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Experimental in people with Shoulder Impingement Syndrome, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 28 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Salah Eid Ahmed Ali (+01158125773, Salah.Eid@Sue.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain intensity level (time frame: 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Aug 2026.

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