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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05678842
Other study ID # GO 22/124
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 16, 2022
Est. completion date December 15, 2022

Study information

Verified date January 2023
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to examine balance parameters and weight distributions at different kneeling positions.


Description:

A cross-sectional study design was used to describe the balance parameters and weight-bearing distributions on knee in different kneeling positions with different ankle conditions. The participants signed informed consent forms before the study was performed on a voluntary basis. Inclusion criteria were defined as being between 18-30 years old and not having knee pain with kneeling. Exclusion criteria were previous history of lower limb pain/pathology, trauma, and/or surgery, any neurological, rheumatological or oncological disorders that would affect balance, have performed high intensity physical activities last 72 hours before test day, and BMI > 25. Balance parameters and weight distribution to each knee were evaluated three times at upright kneeling (UK) and full kneeling (FK) positions, in different ankle conditions (dorsiflexion and plantarflexion) with static balance device. Test-retest ICC values were calculated for all procedures.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date December 15, 2022
Est. primary completion date October 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - being between 18-30 years old - not having knee pain with kneeling Exclusion Criteria: - previous history of lower limb pain/pathology, - trauma, and/or surgery, any neurological, rheumatological or oncological disorders that would affect balance, - have performed high intensity physical activities last 72 hours before test day, - BMI > 25

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Descriptive
Descriptive

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary To investigate balance parameters (postural sway (mm) ) in different kneeling positions. Balance parameters and weight distribution to each knee were evaluated three times at upright kneeling (UK) and full kneeling (FK) positions, in different ankle conditions (dorsiflexion and plantarflexion) with static balance device. HurSmart balance system (HUR smart balance, HUR, Helsinki, Finland) was used for assessed the static balance. Postural sways to antero-posterior (A-P) and medio-lateral (M-L) directions were calculated. one year
Primary weight distributions (kg) in different kneeling positions. weight distribution to each knee were evaluated three times at upright kneeling (UK) and full kneeling (FK) positions, in different ankle conditions (dorsiflexion and plantarflexion) with static balance device. HurSmart balance system (HUR smart balance, HUR, Helsinki, Finland) was used for assessed the weight distribution. one year
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