NCT05439525

Brief Summary

the aim of this study is to investigate the Effect of mulligan technique on sub-acromial space in patients with shoulder impingement syndrome

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 30, 2022

Completed
5 days until next milestone

Study Start

First participant enrolled

July 5, 2022

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2022

Completed
Last Updated

June 30, 2022

Status Verified

June 1, 2022

Enrollment Period

2 months

First QC Date

June 26, 2022

Last Update Submit

June 26, 2022

Conditions

Keywords

mulligan techniquesub-acromial space

Outcome Measures

Primary Outcomes (1)

  • sub-acromial space

    sub-acromial space will be measured by ultrasonography

    up to two weeks

Secondary Outcomes (1)

  • shoulder range of movement

    up to two weeks

Other Outcomes (2)

  • pressure pain threshold

    up to two weeks

  • shoulder function

    up to two weeks

Study Arms (2)

Group A

EXPERIMENTAL

the patient will receive Shoulder complex mobilization with movement three time a week for two weeks

Other: mulligan techniqueOther: conventional therapy

Group B

ACTIVE COMPARATOR

will receive Conventional therapy three times a week for two weeks.

Other: conventional therapy

Interventions

The patient will be in sitting and the therapist stands on the contralateral side of pain, stabilizing the scapula posteriorly with one hand. The head of the humerus is translated posteriorly and laterally with the other hand, along the plane of the glenoid fossa. While the glide is sustained, the patient actively elevates their arm through the plane of abduction or scaption (elevation). Apply 6-10 repetitions in a set, with 3-5 sets in a treatment session the perform mobilization on acromioclavicular and sternoclavicular joint

Group A

1. Flexibility exercises: enhance flexibility of the glenohumeral Posterior capsule, pectoralis muscle, and upper thoracic spine. 2. Strengthen the rotator cuff and scapular stabilizers. 3. Improve upper-quarter postural awareness

Group AGroup B

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • age of patients from 30- 55 years old . Both Male and female.
  • Shoulder pain and two out of four specified objective signs and symptoms:
  • Positive Neer impingement test. Positive Hawkins-Kennedy impingement test. Painful or limitation of active shoulder elevation (flexion, abduction, scaption).
  • Pain or limitation with the functional movement patterns of hand-behind-back or hand-behind-head.

You may not qualify if:

  • Systemic or neurological disorder. Adhesive capsulitis. Cervical radiculopathy. History of shoulder surgery. Corticosteroid injection within the past month Subjects who had received physical therapy treatment for their shoulder within the past three months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Deraya university

Cairo, Egypt

Location

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Central Study Contacts

alshaymaa sh abd el-azeim, lecturer

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
permuted block
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: mulligan and conventional therapy
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator

Study Record Dates

First Submitted

June 26, 2022

First Posted

June 30, 2022

Study Start

July 5, 2022

Primary Completion

August 30, 2022

Study Completion

August 30, 2022

Last Updated

June 30, 2022

Record last verified: 2022-06

Locations