NCT06575855

Brief Summary

This study is basically for the evaluation of comparative effectiveness of instrument assisted soft tissue mobilization IASTM and muscle energy technique MET on Post operative , Randomized clinical trial .

Trial Health

87
On Track

Trial Health Score

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

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 17, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 17, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 17, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 23, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 28, 2024

Completed
Last Updated

August 28, 2024

Status Verified

August 1, 2024

Enrollment Period

2 months

First QC Date

August 23, 2024

Last Update Submit

August 26, 2024

Conditions

Elbow Stiffness

Keywords

Post operative elbow stiffness, MET, IASTM

Outcome Measures

Primary Outcomes (1)

  • VAS and goniometer

    Visual analog scaleThe Visual Analog Scale (VAS) is a 10 cm line with anchor statements on the left (no pain) and on the right (extreme pain) and universal goniometer to measure the range of motion, an instrument that measures angle motion at a joint.

    4 months

Secondary Outcomes (1)

  • DASH questionaire

    4 months

Study Arms (2)

Group A

ACTIVE COMPARATOR

Group A received IASTM as treatment protocol

Other: IASTM

Group B

ACTIVE COMPARATOR

Group B received METs as a treatment protocol

Other: METS

Interventions

IASTMOTHER

Group A received IASTM by using Graston Tool

Group A
METSOTHER

Group B received METs

Group B

Eligibility Criteria

Age30 Years - 50 Years
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • gender both Age:30 to 50 years Who fullfil concent form

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nayyab Goher

Faisalābad, Punjab Province, Pakistan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Patients
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: 28 participants divided in to two groups, Group A and Group B
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Student

Study Record Dates

First Submitted

August 23, 2024

First Posted

August 28, 2024

Study Start

February 17, 2024

Primary Completion

April 17, 2024

Study Completion

June 17, 2024

Last Updated

August 28, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)