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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03782922
Other study ID # 2018-01954
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2018
Est. completion date March 31, 2019

Study information

Verified date December 2018
Source THIM - die internationale Hochschule für Physiotherapie
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, i.e. randomized controlled trial, the effect of an exercise training program on mental and anatomical characteristics of physiotherapy students is measured.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date March 31, 2019
Est. primary completion date February 28, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age =18

- signed consent

- THIM student

- good health status

Exclusion Criteria:

- alcohol

- drugs

- smoking

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise Training Program
10min of coordination and strength training (2-3x per week) during 2-6 weeks

Locations

Country Name City State
Switzerland THIM University of Applied Sciences Landquart

Sponsors (1)

Lead Sponsor Collaborator
THIM - die internationale Hochschule für Physiotherapie

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary d2-R-Test Mental Change from baseline attention and concentration at 4 weeks (objective)
Primary AKA-Questionnaire (attention, concentration, learning ability) Participants fill out a questionnaire about attention, concentration and learning ability. There are five possible answers for each item from 1 (completely disagree) to 5 (completely agree). Change from baseline attention and concentration at 4 weeks (subjective)
Primary M360 - physiological parameter of the spine Participants are measured in different positions (upright, flexion, extension; measured in degrees) to assess position, stability and mobility of the spine. The M360 will be guided along the back and the data will be collected electronically (https://www.idiag.ch/idiag-m360/). Change from baseline position and mobility of the spine at 4 weeks
Primary Pain (Visual Analogue Scale) Participants can use this scale to classify their pain from "No pain" and "Maximum pain imaginable" by means of a slider. Change from baseline pain (back) at 4 weeks
Primary FAW-Questionnaire (Actual physical well-being) Participants fill out a questionnaire with 58 questions. Each question has five possible answers from 0 (completely disagree) to 4 (completely agree). The highter the score the better the actual physical well-being. Change from baseline physical well-being at 4 weeks
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