Effect of Vojta Therapy on Covid-19 Respiratory Disease
Primary Purpose
COVID-19 Acute Respiratory Distress Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Respiratory physiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for COVID-19 Acute Respiratory Distress Syndrome focused on measuring Vojta therapy, Respiratory physiotherapy
Eligibility Criteria
Inclusion Criteria:
- respiratory disease by covid-19
Exclusion Criteria:
- patient older than 75 years
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Vojta Therapy
Control Group
Arm Description
Reflex turn first phase: Patient positioned supine with legs flexed 30º-45º. The pectoral area is stimulated for five minutes on each side x 2 consecutive times. Total 20 minutes per session.
.Inspiratory techniques, mucociliary clearance techniques (expiratory). Use of inspiratory and expiratory incentives. Employment of mechanical assistants
Outcomes
Primary Outcome Measures
SpO2
Oxygen saturation
Breathing frequency
frequency of respiratory cycles per minute
Stay time
Days of stay in the intermediate respiratory care unit
Secondary Outcome Measures
Full Information
NCT ID
NCT05031858
First Posted
August 28, 2021
Last Updated
August 30, 2021
Sponsor
NUMEN Foundation
Collaborators
Hospital de Emergencias Enfermera Isabel Zendal de Madrid
1. Study Identification
Unique Protocol Identification Number
NCT05031858
Brief Title
Effect of Vojta Therapy on Covid-19 Respiratory Disease
Official Title
Effect of Vojta Therapy in Respiratory Disease Caused by SARS-CoV-2. Randomized Controlled Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 25, 2021 (Anticipated)
Primary Completion Date
December 20, 2021 (Anticipated)
Study Completion Date
April 15, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
NUMEN Foundation
Collaborators
Hospital de Emergencias Enfermera Isabel Zendal de Madrid
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Vojta therapy is a physiotherapy intervention with scientific evidence in respiratory pathologies in children and proven in adults. In this pilot study with an RCT design, its effect in adult patients with respiratory pathology caused by the SARS-CoV-2 virus will be studied. The non-invasive and non-painful technique consists of applying tolerable pressure to specific areas of the patient's body. The objective is to activate, in a reflex way, the ventilatory physiology. It is compared with the conventional respiratory physiotherapy approach.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19 Acute Respiratory Distress Syndrome
Keywords
Vojta therapy, Respiratory physiotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Vojta Therapy
Arm Type
Experimental
Arm Description
Reflex turn first phase: Patient positioned supine with legs flexed 30º-45º. The pectoral area is stimulated for five minutes on each side x 2 consecutive times. Total 20 minutes per session.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
.Inspiratory techniques, mucociliary clearance techniques (expiratory). Use of inspiratory and expiratory incentives. Employment of mechanical assistants
Intervention Type
Other
Intervention Name(s)
Respiratory physiotherapy
Intervention Description
Respiratory physiotherapy
Primary Outcome Measure Information:
Title
SpO2
Description
Oxygen saturation
Time Frame
3 weeks
Title
Breathing frequency
Description
frequency of respiratory cycles per minute
Time Frame
3 weeks
Title
Stay time
Description
Days of stay in the intermediate respiratory care unit
Time Frame
3 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
respiratory disease by covid-19
Exclusion Criteria:
patient older than 75 years
12. IPD Sharing Statement
Learn more about this trial
Effect of Vojta Therapy on Covid-19 Respiratory Disease
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