- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06224491
Non Motoric Reactions in Vojta Reflex Locomotion (VojtaRL)
Relationship Between Stress and Anxiety Levels and Ratings of Accompanying Non-occupational Symptoms in Vojta's Comprehensive RL Response
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Praha, Czechia, 162 52
- Faculty of Physical Education and Sport
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
These will be healthy adult women. The expected number of participants is 20-30. To participate in the study, participants must agree to participate voluntarily.
Exclusion Criteria:
Contraindications for participation include psychiatric illness, cancer, acute inflammatory diseases, and pregnancy. Persons with signs of acute illness or injury or in recovery from acute illness or injury will not be eligible for testing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Sham Comparator: Placebo tactile stimulation
From a standardized starting position for 10 minutes tactile contact in the area outside the description of reflex zones in reflex locomotion according to Vojta.
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Tactile stimulation according to Vojta´s reflex locomotion
Other Names:
|
Experimental: Reflex locomotion zone stimulation
From a standardized starting position tactile stimulation in the area of the zone in reflex locomotion according to Vojta for 10 minutes .
|
Tactile stimulation according to Vojta´s reflex locomotion
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Non-motor responses during tactile stimulation in reflex locomotion according to Vojta
Time Frame: 10 minutes tactile stimulation
|
The Trigno Wireless EMG System Delsys will be used to measure electrical muscle activity.
The SP-10 Pocket Spirometer Gima and wireless ECG will be used to measure changes in breathing and circulation.
In addition, the DASS-42 and POMS questionnaires will be used.
|
10 minutes tactile stimulation
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Collaborators and Investigators
Investigators
- Study Chair: Zuzana Charvátová, PhD., Faculty of Physical Education and Sport Charles University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 122111PRG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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