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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04324242
Other study ID # GO 16/808
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 13, 2020
Est. completion date September 15, 2020

Study information

Verified date April 2020
Source Hacettepe University
Contact Esra Dülger
Phone +905395821958
Email esradulger@hacettepe.edu.tr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Transversus abdominis (TrA) is an important muscle for spinal stabilization. Abdominal draw-in maneuver (ADIM) is a method that selectively activates TrA without activating external oblique (EO) and internal oblique (IO) muscles. Individuals with low back pain may have some troubles to understand proper contraction of TrA. Therefore, to contract the TrA, two different feedback techniques have been used to instruct. In this observational study we aim to investigate the effects of two different biofeedback methods to teach patients the proper activation of TrA muscle using ADIM. We aim to find out the differences between visual and traditional tactile biofeedback and decide which one is practical and easy to teach the patients in clinical environment.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date September 15, 2020
Est. primary completion date April 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria:

- healthy volunteers between ages of 18-25

Exclusion Criteria:

- Volunteers excluded if they had (1) history of LBP, (2) spinal or abdominal surgeries, (3) neuromusculer or romatologic diseases. Each volunteer gave their informed consent.

Study Design


Intervention

Other:
abdominal hallowing maneuver
abdominal hallowing maneuver includes tucking navel in and up. To be able to control the effect of breathing it was instructed to start the maneuver at the end of the expiration. During the maneuver it was instructed to focus on increasing the thickness of TrA without increasing the thickness of IO and EO

Locations

Country Name City State
Turkey Hacettepe University Ankara Çankaya

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary thickness change in TrA muscle thickness change in TrA muscle 1 month
Secondary thickness change in EO muscle thickness change in EO muscle 1 month
Secondary thickness change in IO muscle thickness change in IO muscle 1 month
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