NCT06420882

Brief Summary

Chondromalacia patella (CMP) is a common condition in patients presenting to healthcare units with anterior knee pain (1).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 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

May 15, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

May 15, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

May 20, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 6, 2024

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 3, 2024

Completed
Last Updated

September 19, 2024

Status Verified

May 1, 2024

Enrollment Period

3 months

First QC Date

May 15, 2024

Last Update Submit

September 3, 2024

Conditions

Outcome Measures

Primary Outcomes (5)

  • WOMAC

    The Turkish version of the WOMAC scale will be used to evaluate the pain, stiffness and physical function of the individuals included in the study. The score of each section is calculated within itself and the total score varies between 0 and 100. High scores indicate an increase in pain and stiffness and impairment in physical function (12,13).

    3 weeks

  • Stair climbing test

    Stair ascent and descent test: The patient's ascent and descent time of the 11-step staircase with a height of 14 cm and a depth of 29 cm were recorded separately with a stopwatch.

    3 weeks

  • Range of motion of the joint

    Knee joint range of motion will be measured with a goniometer.

    3 weeks

  • Star balance test

    The test is a simple but time-consuming test in terms of its application and is used to measure dynamic postural balance (1). The test is based on the ability to reach the farthest possible distance on the supporting leg with the free foot in 8 different directions

    3 weeks

  • Horizontal jump test

    They jump to the farthest distance they can jump using their single and double legs and the best result obtained after at least 2 trials is recorded in cm. In this test, it should be noted that when contact with the ground after the jump, the measurement should be made at the heel level of the back foot, which is close to the starting line. Another point to be considered is that the participant should be stationary at the starting line. The participant cannot come to the line running and jump. But it is allowed to make a springing movement in front of the line

    3 weeks

Study Arms (2)

The rehabilitation group.

EXPERIMENTAL

rehabilitation group.

Other: The experimental group.

The home exercise group

ACTIVE COMPARATOR

The home exercise group

Other: The home exercise group

Interventions

In the experimental group, in addition to home exercises, patella mobilization, muscle strengthening exercises, range of motion exercises and home exercises will be performed 3 days a week for 3 sessions with a therapist.

The rehabilitation group.

Participants in both groups will be included in a 3-week treatment programme.

The home exercise group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • years of age.
  • Being diagnosed with chondromalacia
  • Participate in the work on a voluntary basis
  • Obtaining informed consent from them

You may not qualify if:

  • Fracture, ligament or muscle tear in the lower extremity within the last 3 months.
  • Having a systemic disease
  • Having a serious injury in the last 3 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gamze Demircioğlu

Istanbul, None Selected, 34353, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Knee Injuries

Condition Hierarchy (Ancestors)

Leg InjuriesWounds and Injuries

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 15, 2024

First Posted

May 20, 2024

Study Start

May 15, 2024

Primary Completion

August 6, 2024

Study Completion

September 3, 2024

Last Updated

September 19, 2024

Record last verified: 2024-05

Data Sharing

IPD Sharing
Will not share

Locations