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Comparison Of Effectiveness of Mobilization With Movement (MWM) and Kelternborn Treatment Technique to Increase ROM, Reducing Pain in Patient of ACL Reconstruction

Comparison Of Effectiveness of Mobilization With Movement (MWM) and Kelternborn Treatment Technique to Increase ROM, Reducing Pain in Patient of ACL Reconstruction

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05873101
Enrollment
22
Registered
2023-05-24
Start date
2023-04-01
Completion date
2023-08-31
Last updated
2023-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

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

Interventions

Mobilization With Movement

DIAGNOSTIC_TESTKelternborn Treatment Technique

Kelternborn Treatment Technique

Sponsors

Superior University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* • 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.

Exclusion criteria

* • 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.)

Design outcomes

Primary

MeasureTime frame
Goniometer (Range of Motion)6 Months
Visual Analog Scale ( VAS)6 Months

Countries

Pakistan

Contacts

Primary ContactShahzaib Sajjad, DPT
dptm-f17-063@superior.edu.pk+923009425452

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026