NCT06150170

Brief Summary

Evaluation of the Efficiency of Propioceptive Study According to Radiological Stages in Patients with Knee Osteoarthritis

Trial Health

87
On Track

Trial Health Score

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

Enrollment
34

participants targeted

Target at below P25 for not_applicable knee-osteoarthritis

Timeline
Completed

Started Nov 2023

Shorter than P25 for not_applicable knee-osteoarthritis

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

First Submitted

Initial submission to the registry

November 21, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

November 21, 2023

Completed
8 days until next milestone

First Posted

Study publicly available on registry

November 29, 2023

Completed
22 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 21, 2023

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 5, 2024

Completed
Last Updated

July 9, 2024

Status Verified

July 1, 2024

Enrollment Period

1 month

First QC Date

November 21, 2023

Last Update Submit

July 7, 2024

Conditions

Keywords

knee osteoarthritisrehabilitationexercisephysiotherapypropioception

Outcome Measures

Primary Outcomes (1)

  • The Western Ontario and McMaster Universities Arthritis Index (WOMAC)

    The scale consists of 3 main headings and 24 questions. It is scored between 0 and 100. There is a negative correlation between scoring and functionality.

    Evaluation will be performed before treatment and after 4 weeks rehabilitation program.

Secondary Outcomes (9)

  • Visual Analogue Scale (VAS)

    Evaluation will be performed at Baseline (before treatment) and 4 weeks

  • Pressure Pain Threshold Measurement

    Evaluation will be performed at Baseline (before treatment) and 4 weeks

  • Range of Motion (ROM)

    Evaluation will be performed at Baseline (before treatment) and 4 weeks

  • Timed Up and Go Test (TUG)

    Evaluation will be performed at Baseline (before treatment) and 4 weeks

  • Manual Muscle Test

    Evaluation will be performed at Baseline (before treatment) and 4 weeks

  • +4 more secondary outcomes

Study Arms (2)

Group 1

EXPERIMENTAL

This group includes patients with grade 1 and grade 2 knee osteoarthritis.

Other: Proprioceptive training

Group 2

EXPERIMENTAL

This group includes patients with grade 3 and grade 4 osteoarthritis.

Other: Proprioceptive training

Interventions

Proprioceptive exercises were applied to both groups. In addition to these exercises, balance, coordination and strengthening exercises will also be applied to both groups.

Group 1Group 2

Eligibility Criteria

Age35 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosed with knee osteoarthritis by a specialist physician using MRI, US or radiography and physical examination.
  • Being between the ages of 35-70
  • Stage 1-2-3-4 according to Kellegran Lawrence (K-L) in radiological examination

You may not qualify if:

  • Having active synovitis
  • Having received physical therapy in the last 6 months
  • Those with neurological problems that affect walking
  • Those with serious respiratory, central, peripheral, vascular and uncontrolled metabolic problems that will prevent exercise
  • Has had lower extremity surgery in the past
  • Intra-articular steroid injections within the last 6 months
  • Using psychoactive drugs
  • Those with serious vision, hearing and speech disorders
  • Patients with vestibular dysfunction will not be included in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Health Sciences University

Üsküdar, Istanbul, 34668, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Osteoarthritis, KneeMotor Activity

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesBehavior

Study Officials

  • Sibel Gayretli Atan

    sssibel_38@hotmail.com

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist

Study Record Dates

First Submitted

November 21, 2023

First Posted

November 29, 2023

Study Start

November 21, 2023

Primary Completion

December 21, 2023

Study Completion

April 5, 2024

Last Updated

July 9, 2024

Record last verified: 2024-07

Locations