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Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post FacilitationStretch in Shoulder Impingement Syndrome

Primary Purpose

Shoulder Impingement Syndrome

Status

Completed

Phase

Not Applicable

Locations

Pakistan

Study Type

Interventional

Intervention

KAlternborn Joint Mobilization

Post stretch Facilitation Technique

About this trial

This is an interventional treatment trial for Shoulder Impingement Syndrome

Eligibility Criteria

25 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Both male and female Age 25 to 45 Diagnosed Rotator cuff impingement from ortho, neuro and musculoskeletal department Hawkin kennedy test positive Neer's test positive Jobe's test positive Exclusion Criteria: Cervical spine disorder Fractures Major upper limb surgery Tumor or wound Diagnosed acromial malformations

Sites / Locations

Al Nafees Medical Hospital, Islamabd

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

control group

experimental group

Arm Description

kalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week.

Post stretch facilitation technique will be administered for total of 8 weeks at the rate of 2 session per week.

Outcomes

Primary Outcome Measures

Goniometer

This is a instrument designed to evaluate the joint range of motion. Greater ranges mean more mobility of joint and less means more restriction

Shoulder Pain and Disability Index

Used to assess the patients level of pain and the ADLs which are affected. O score means no dysfuction of joint and higer score means more dysfuction

Secondary Outcome Measures

Full Information

NCT ID

NCT05871944

First Posted

May 13, 2023

Last Updated

May 22, 2023

Sponsor

Neuro Counsel Hospital, Pakistan

Collaborators

Al Nafees Medical Hospital, Islamabad, National Institute of Rehabilitation Medicine, Islamabad, Pakistan

1. Study Identification

Unique Protocol Identification Number

NCT05871944

Brief Title

Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post FacilitationStretch in Shoulder Impingement Syndrome

Official Title

Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post Facilitation Stretch in Shoulder Impingement Syndrome

Study Type

Interventional

2. Study Status

Record Verification Date

May 2023

Overall Recruitment Status

Completed

Study Start Date

January 5, 2023 (Actual)

Primary Completion Date

May 4, 2023 (Actual)

Study Completion Date

May 4, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Neuro Counsel Hospital, Pakistan

Collaborators

Al Nafees Medical Hospital, Islamabad, National Institute of Rehabilitation Medicine, Islamabad, Pakistan

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

This study is a experimental one to observe the efficacy of joint mobilization and post facilitation techniques in shoulder impingement syndrome

Detailed Description

his study is a experimental one to observe the efficacy of Kalternborn end range joint mobilization and post facilitation techniques in shoulder impingement syndrome. Goniometer, shoulder disability index will be the tool used for evaluation

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Shoulder Impingement Syndrome

7. Study Design

Primary Purpose

Treatment

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Model Description

Two groups will be formed. one group will receive joint mobilization technique and other will get post facilitation stretch technique

Masking

Participant

Masking Description

This will be single blind randomized control clinical trail in which just participant will be unware about which group he/she is included

Allocation

Randomized

Enrollment

20 (Actual)

8. Arms, Groups, and Interventions

Arm Title

control group

Arm Type

Active Comparator

Arm Description

kalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week.

Arm Title

experimental group

Arm Type

Experimental

Arm Description

Post stretch facilitation technique will be administered for total of 8 weeks at the rate of 2 session per week.

Intervention Type

Other

Intervention Name(s)

KAlternborn Joint Mobilization

Intervention Description

This is a join mobilization technique to reduce the joint stiffness and help in improving joint range of motion

Intervention Type

Other

Intervention Name(s)

Post stretch Facilitation Technique

Intervention Description

This is a PNF techniques used to relax the muscles and help in getting more free range of restricted joint

Primary Outcome Measure Information:

Title

Goniometer

Description

This is a instrument designed to evaluate the joint range of motion. Greater ranges mean more mobility of joint and less means more restriction

Time Frame

4 weeks

Title

Shoulder Pain and Disability Index

Description

Used to assess the patients level of pain and the ADLs which are affected. O score means no dysfuction of joint and higer score means more dysfuction

Time Frame

4 weeks

10. Eligibility

Sex

All

Minimum Age & Unit of Time

25 Years

Maximum Age & Unit of Time

45 Years

Accepts Healthy Volunteers

Eligibility Criteria

Facility Information:

Facility Name

Al Nafees Medical Hospital, Islamabd

City

Islamabad

State/Province

Federal

ZIP/Postal Code

44000

Country

Pakistan

12. IPD Sharing Statement

Plan to Share IPD

Undecided

IPD Sharing Plan Description

Have not decided yet about this.

Learn more about this trial

Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post FacilitationStretch in Shoulder Impingement Syndrome

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