Exercise Training Programm for Physiotherapy Students
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03782922 |
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Recruitment Status :
Completed
First Posted : December 20, 2018
Last Update Posted : April 11, 2019
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Healthy Student Physical Therapy | Other: Exercise Training Program | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 80 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Triple (Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Prevention |
| Official Title: | Effect of an Exercise Training Programm on Mental and Anatomical Characteristics of Physiotherapy Students - a Randomized Controlled Trial |
| Actual Study Start Date : | December 1, 2018 |
| Actual Primary Completion Date : | February 28, 2019 |
| Actual Study Completion Date : | March 31, 2019 |
| Arm | Intervention/treatment |
|---|---|
| Experimental: Exercise Training Program |
Other: Exercise Training Program
10min of coordination and strength training (2-3x per week) during 2-6 weeks |
| No Intervention: Control |
- d2-R-Test [ Time Frame: Change from baseline attention and concentration at 4 weeks (objective) ]Mental
- AKA-Questionnaire (attention, concentration, learning ability) [ Time Frame: Change from baseline attention and concentration at 4 weeks (subjective) ]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).
- M360 - physiological parameter of the spine [ Time Frame: Change from baseline position and mobility of the spine at 4 weeks ]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/).
- Pain (Visual Analogue Scale) [ Time Frame: Change from baseline pain (back) at 4 weeks ]Participants can use this scale to classify their pain from "No pain" and "Maximum pain imaginable" by means of a slider.
- FAW-Questionnaire (Actual physical well-being) [ Time Frame: Change from baseline physical well-being at 4 weeks ]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.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- age ≥18
- signed consent
- THIM student
- good health status
Exclusion Criteria:
- alcohol
- drugs
- smoking
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03782922
| Switzerland | |
| THIM University of Applied Sciences | |
| Landquart, Switzerland, 7302 | |
| Responsible Party: | THIM - die internationale Hochschule für Physiotherapie |
| ClinicalTrials.gov Identifier: | NCT03782922 |
| Other Study ID Numbers: |
2018-01954 |
| First Posted: | December 20, 2018 Key Record Dates |
| Last Update Posted: | April 11, 2019 |
| Last Verified: | December 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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exercise anatomical mental training program |

