NCT06447142

Brief Summary

This randomized-controlled trial aims to compare the effect of open kinetic chain and closed kinetic chain strengthening exercises on pain, function, and health-related quality of life in degenerative meniscus tears.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
56

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 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

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 3, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 6, 2024

Completed
4 days until next milestone

Study Start

First participant enrolled

June 10, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 25, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 10, 2025

Completed
Last Updated

June 13, 2025

Status Verified

June 1, 2024

Enrollment Period

5 months

First QC Date

June 3, 2024

Last Update Submit

June 10, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Knee Injury and Osteoarthritis Outcome Score (KOOS)

    Short-term and long-term symptoms and function will be assessed with the Knee injury and Osteoarthritis Outcome Score (KOOS) that is developed as an extension of the WOMAC Osteoarthritis Index. The score is a percentage score from 0 to 100, 0 representing extreme problems and 100 representing no problems.

    Baseline

Secondary Outcomes (11)

  • Knee Injury and Osteoarthritis Outcome Score (KOOS)

    At the end of 8-week intervention

  • Visual Analogue Scale (VAS)

    Baseline

  • Visual Analogue Scale (VAS)

    At the end of 8-week intervention

  • Active Range of Motion

    Baseline

  • Active Range of Motion

    At the end of 8-week intervention

  • +6 more secondary outcomes

Study Arms (2)

Open Kinetic Chain Exercise Group

EXPERIMENTAL

Each subject in Open Kinetic Chain Exercise Group will receive a treatment protocol consisting of stretching exercises, open kinetic chain strengthening exercises, and functional exercises for the knee and hip.

Other: Open kinetic chain strengthening exercise

Closed Kinetic Chain Exercise Group

ACTIVE COMPARATOR

Each subject in Closed Kinetic Chain Exercise Group will receive a treatment protocol consisting of stretching exercises, closed kinetic chain strengthening exercises, and functional exercises for the knee and hip.

Other: Closed kinetic chain strengthening exercise

Interventions

A web-based 8-week exercise program consisting of stretching exercises, open kinetic chain strengthening exercises, and functional exercises for the knee and hip will be performed.

Open Kinetic Chain Exercise Group

A web-based 8-week exercise program consisting of stretching exercises, closed kinetic chain strengthening exercises, and functional exercises for the knee and hip will be performed.

Closed Kinetic Chain Exercise Group

Eligibility Criteria

Age35 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being aged between 35 and 65 years
  • Having the degenerative meniscus tear in at least one knee
  • Having body mass index in the range of 18-30 kg/m2
  • Feeling the pain that lasts for at least 2 months
  • Having grade 1 or grade 2 degenerative meniscal tear diagnosed by an orthopedic specialist according to the MRI results
  • Access to the internet via a computer or smartphone
  • Ability to read and write in Turkish

You may not qualify if:

  • Having undergone arthroscopic partial meniscectomy surgery due to degenerative meniscal tear
  • Participating in a physiotherapy program for degenerative meniscal tear in the last 12 weeks
  • Have received steroid injections in the last 6 months
  • Accompanying conditions such as injury to the surrounding ligaments, congenital anomaly in the affected knee, coxarthrosis and spinal stenosis
  • Presence of any systemic disorder that may affect assessment parameters
  • Any health condition that may prevent participation in physical activity or an exercise program (e.g., severe cardiovascular, respiratory, neurological, or musculoskeletal disorders)
  • Failure to cooperate with assessments

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University-Cerrahpasa

Istanbul, Bakırkoy, 34147, Turkey (Türkiye)

Location

Study Officials

  • Tansu Birinci, PT, PhD

    Istanbul University - Cerrahpasa

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 3, 2024

First Posted

June 6, 2024

Study Start

June 10, 2024

Primary Completion

October 25, 2024

Study Completion

January 10, 2025

Last Updated

June 13, 2025

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations