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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06264648
Other study ID # AIBU-FTR-OOP-04
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 3, 2023
Est. completion date October 20, 2023

Study information

Verified date February 2024
Source Abant Izzet Baysal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is planned for searching physiotherapists palpation abilities. There were 2 groups of physiotherapists. They were asked for to push target pressures. After making some exercise, the assesment was done again.


Description:

2 groups of physiotherapists with different fields of experience were attended to study. Fingers are positioned on the marked area at the center point of the scale. Therapists were asked to apply pressure to the scale with estimated weights of 0.5 kg, 1 kg, 2 kg and 4 kg. In each measurements, the value on the scale was recorded without being shown to the participants. After the measurements, the participants were made to experiment when the digital screen can be seen, in order to teach the physiotherapists how much pressure they applied to reach the target weight. Participants were given a total of 10 minutes for the trials. Then, the digital screen was hidden again, and the therapist was asked to apply 0.5 kg, 1 kg, 2 kg and 4 kg weight in a randomized order and maintain that pressure for 5 seconds. The weight fixed by the therapist for 5 seconds was noted by the researcher; the participant was not informed about the values on the digital screen.


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date October 20, 2023
Est. primary completion date June 16, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 22 Years and older
Eligibility Inclusion Criteria: - Willing to participate, - Active working patients as a physiotherapists pediatric, neurologic, orthopedic physiotherapy, manual therapy or osteopathy. Exclusion Criteria: - Having a neurological disease (multiple sclerosis, polyneuropathy, etc.) -Having a disease that may cause neurological deficit in the upper extremity (cervical myelopathy, carpal tunnel syndrome, pronator teres syndrome, cubital tunnel syndrome, --- - Guyon canal syndrome) - Refuse to participate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pressure sensitivity education
Therapists were asked to apply pressure to the scale with estimated weights of 0.5 kg, 1 kg, 2 kg and 4 kg. In each measurement, the value shown on the scale was recorded without being shown to the participant.After the measurements, the participants were made to experiment when the digital screen can be seen, in order to teach the physiotherapists how much pressure they applied to reach the target weight. Participants were given a total of 10 minutes for the trials. Then, the digital screen was hidden again, and the therapist was asked to apply 0.5 kg, 1 kg, 2 kg and 4 kg weight in a randomized order and maintain this pressure for 5 seconds. The weight fixed by the therapist for 5 seconds was noted by the researcher; the participant was not informed about the values on the digital screen.

Locations

Country Name City State
Turkey Faculty of Health Sciences Bolu Abant Izzet Baysal University Bolu

Sponsors (1)

Lead Sponsor Collaborator
Abant Izzet Baysal University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement Palpation Pressure with Digital Scale The digital scale will used to assess the palpation pressure of participants. This digital scale is designed for a measurement range of 1-10.000 gr. Palpation pressures will measure at baseline and after education to see whether any changes. baseline
Primary Measurement Palpation Pressure with Digital Scale The digital scale will used to assess the palpation pressure of participants. This digital scale is designed for a measurement range of 1-10.000 gr. Palpation pressures will measure at baseline and after education to see whether any changes. 10 minute after pressure sensitivity education
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