NCT07333092

Brief Summary

The aim of this study is to investigate the effects of proprioceptive exercises on balance, kinesiophobia, and functionality after anterior cruciate ligament surgery.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress52%
Jan 2026Aug 2026

First Submitted

Initial submission to the registry

December 30, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 12, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

January 15, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 20, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2026

Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

5 months

First QC Date

December 30, 2025

Last Update Submit

January 15, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Lysholm Knee Scoring Scale

    The Lysholm scale was developed for use by physicians and has been verified in patients with Anterior Cruciate Ligament and meniscal injuries. It's also been approved as a patient-administered tool for assessing symptoms and function in people who have had a variety of knee injuries. The Lysholm scale assesses the domains of symptoms and complaints, as well as functioning in daily activities, however, it doesn't assess the area of sports and recreational activities. There are 8 items on this questionnaire and graded on a scale of 0 to 100, with higher scores suggesting fewer symptoms and better function

    14 weeks

  • Tampa Kinesiophobia Questionnaire

    Tampa Kinesiophobia Questionnaire is a 17-question questionnaire that assesses avoidance of injury and fear of movement. The scale is scored using a Likert scale (1 = Strongly disagree, 4 = Strongly agree). Items 4, 8, 12 and 16 are reversed to calculate the total score of the scale. The total score is between 17 and 68. As the score of the person increases, it is understood that their kinesiophobia is high. A total score higher than 37 is considered as high kinesiophobia. However, since not every item of the questionnaire addresses patients with headache in this study, some questions were removed, some questions were edited and some questions were added to create a kinesiophobia questionnaire for headache. The newly created questionnaire consists of 23 items. Again, it is scored using a Likert scale with "1 = Strongly disagree, 4 = Strongly agree". As the score increases, it is understood that the level of kinesiophobia is high

    14 weeks

  • Y Balance Test

    The Y Balance Test will be used to assess dynamic balance by measuring reach distances in three directions (anterior, posteromedial, and posterolateral) while standing on one leg. Each direction will be tested three times, and the average reach distance will be normalized to leg length. A composite score will be calculated and expressed as a percentage to evaluate overall dynamic balance capacity. Higher scores indicate better balance performance.

    14 weeks

Study Arms (2)

control group

ACTIVE COMPARATOR

balance exercises

Other: control

exercise group

EXPERIMENTAL

balance exercises + proprioceptive exercises

Other: controlOther: exercise

Interventions

In addition to balance exercises, proprioceptive exercises will be performed.

exercise group
controlOTHER

Patients will only be given balance exercises that are currently available at the hospital.

control groupexercise group

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being between 20-40 years of age
  • Having undergone anterior cruciate ligament (ACL) surgery
  • Being in the 2nd week of rehabilitation after ACL surgery

You may not qualify if:

  • Having a concomitant meniscus injury
  • Having a concomitant medial collateral ligament injury
  • Being in the 1st week of rehabilitation after ACL surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Şanlıurfa Mehmet Akif İnan Health Application and Research Center

Sanliurfa, Turkey (Türkiye)

RECRUITING

Related Publications (3)

  • Zult T, Gokeler A, van Raay JJAM, Brouwer RW, Zijdewind I, Farthing JP, Hortobagyi T. Cross-education does not accelerate the rehabilitation of neuromuscular functions after ACL reconstruction: a randomized controlled clinical trial. Eur J Appl Physiol. 2018 Aug;118(8):1609-1623. doi: 10.1007/s00421-018-3892-1. Epub 2018 May 23.

    PMID: 29796857BACKGROUND
  • Erayata BN, Menek B. Investigating the effects of percussion massage therapy on pain, functionality, muscle diameter, and proprioception in individuals with ACL reconstruction: a randomized controlled trial. PLoS One. 2025 Mar 26;20(3):e0319731. doi: 10.1371/journal.pone.0319731. eCollection 2025.

    PMID: 40138389BACKGROUND
  • Keays SL, Bullock-Saxton JE, Newcombe P, Bullock MI. The effectiveness of a pre-operative home-based physiotherapy programme for chronic anterior cruciate ligament deficiency. Physiother Res Int. 2006 Dec;11(4):204-18. doi: 10.1002/pri.341.

    PMID: 17236528BACKGROUND

MeSH Terms

Conditions

Anterior Cruciate Ligament Injuries

Interventions

Exercise

Condition Hierarchy (Ancestors)

Knee InjuriesLeg InjuriesWounds and Injuries

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Ayşe ŞAN

    Uskudar University

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assoc.Prof.Dr.

Study Record Dates

First Submitted

December 30, 2025

First Posted

January 12, 2026

Study Start

January 15, 2026

Primary Completion (Estimated)

June 20, 2026

Study Completion (Estimated)

August 20, 2026

Last Updated

January 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations