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Clinical Trial Summary

For the breathing intervention, participants completed two experimental sessions at least two weeks apart. The experimental sessions were randomized between the slow-breathing condition (6 breaths/min) or the control breathing condition (12 breaths/min). Breathing interventions were 15 minutes in length and completed with the assistance of the breathing app, Breathe Deep (Mineev, Bizi Apps LLC). The breathing intervention is currently completed. The reliability and validity study of AFAS is ongoing. This is a one-time visit for participants in which participants will undergo screening of sensation and movement as well as fill in some questionnaires.


Clinical Trial Description

All participants had two visits for the breathing exercise. The only planned intervention was the breathing exercise, which is now concluded. The protocol for the breathing intervention was as follows: The breathing protocol lasted 15 minutes. It was a guided breathing awareness session with a registered nurse (PhD student) who is also trained in integrative therapies and yoga instruction. In parallel, during one of the visits the reliability and validity of a new scale for stroke to measure quality of movement and body awareness is tested. This part is still ongoing and thus this becomes a one-time visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03328468
Study type Interventional
Source University of Minnesota
Contact Ann Van de Winckel, PhD, MS, PT
Phone 612-625-1191
Email avandewi@umn.edu
Status Recruiting
Phase N/A
Start date December 30, 2017
Completion date October 1, 2024

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