Comparison Of Effectiveness of Mobilization With Movement (MWM) and Kelternborn Treatment Technique to Increase ROM, Reducing Pain in Patient of ACL Reconstruction
1 other identifier
interventional
22
1 country
1
Brief Summary
To determine the Comparison Of Effectiveness of Mobilization With Movement (MWM) and Kelternborn Treatment Technique to Increase ROM, Reducing Pain in Patient of ACL Reconstruction
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable pain
Started Apr 2023
Shorter than P25 for not_applicable pain
1 active site
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
March 18, 2023
CompletedStudy Start
First participant enrolled
April 1, 2023
CompletedFirst Posted
Study publicly available on registry
May 24, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2023
CompletedMay 24, 2023
May 1, 2023
2 months
March 18, 2023
May 23, 2023
Conditions
Outcome Measures
Primary Outcomes (2)
Goniometer (Range of Motion)
6 Months
Visual Analog Scale ( VAS)
6 Months
Study Arms (2)
Mobilization With Movement (MWM)
OTHERKelternborn Treatment Technique
EXPERIMENTALInterventions
Mobilization With Movement
Kelternborn Treatment Technique
Eligibility Criteria
You may qualify if:
- Subjects with age group between 20 to 60 years with sedentary lifestyle were included.
- Both males and females were included.
- Patients with diagnosed Tight hamstrings having knee extension less than 160º with the hip at 90º flexion.
- Patients with decreased ROM at the knee joint.
- Patients with reduced straight leg raise.
- Patients with pain in posterior compartment of thigh.
- Asymptomatic patients will be included.
You may not qualify if:
- Patients with prolapsed disc were excluded.
- Patients with lower extremity injuries (strain, sprain, ligament injuries, etc.) in last 6 months were excluded.
- Patients with severe hamstring injury either acute or chronic were excluded.
- Patients with visual acute swelling in the region of hamstring muscle
- Patients with fracture of any type and area.
- Patients with dislocations or subluxations present were excluded.
- Patient recommended for TKR of knee joint.
- Patients with any neurological disease like lumbar/cervical herniation, polyneuropathy, scoliosis etc.)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Superior University
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 18, 2023
First Posted
May 24, 2023
Study Start
April 1, 2023
Primary Completion
June 1, 2023
Study Completion
August 1, 2023
Last Updated
May 24, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share