RespiraConNosotros:a Mobile Application for COVID-19 Respiratory Rehabilitation.

Covid19 Clinical Trial

Official title:

RespiraConNosotros: Creation and Implementation of a Mobile Application for the Rehabilitation of Patients With Respiratory Sequelae of the SARS-CoV-2 (COVID-19)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04703478
• Other study ID #: CovidSal02
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 20, 2021
• Est. completion date: April 20, 2021

Study information

• Verified date: January 2021
• Source: University of Salamanca
• Contact: Beatriz M Bermejo-Gil, Prof.
• Phone: +34 622 289 468
• Email: beatriz.bermejo[@]usal.es
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Platform with a mobile application to encourage the performance of respiratory exercises, controlled and supervised by physiotherapists. It also includes recommendations, frequently asked questions and the possibility of contacting by chat or video calls with experts to solve possible doubts.

Currently, the application is ready for use, the registration of users and professionals is enabled and have 20 exercises divided into three intensity levels.

It is available for all platforms (PC, ANDROID, iOS). presents a simple deployment, accessible to the entire population and does not require installation.

In the future, investigators will include more languages, a greater variety of exercises and even other types of therapies. Investigators will also carry out the adaptation to functional diversity with subtitles and voice commands.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: April 20, 2021
• Est. primary completion date: April 20, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Respiratory affectation diagnosis

• Internet access to run the application

Exclusion Criteria:

• Presence of contraindications to physical exercise or the lack of comprehensive ability to access the application will be considered.

Related Conditions & MeSH terms

• Covid19

Intervention

Other:
• Breathing exercise
Participants will carry out a breathing exercise program through the RespiraConNosotros mobile application. They will be asked to carry out the proposed exercises with a frequency of 3 times a week for 3 months.

Locations

Country	Name	City	State
Spain	Ines Llamas-Ramos	Salamanca

Sponsors (1)

Lead Sponsor	Collaborator
University of Salamanca

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rating of perceived exertion (Borg Scale)	Scale from 1-10 points. Where number 1 means very light activity and 10, represents an extreme intensity of activity.	10 minutes.
Primary	Level of satisfaction and acceptability.	A Likert-type scale will be used. 1-Not Satisfied to 5-Extremely satisfied.	20 minutes.
Primary	St. George's Respiratory Questionnaire, SGRQ	scale from 0-100 points.Where higher scores mean worse outcomes.	40 minutes.
Secondary	Age	The date of birth will be registered in order to calculate the age of the participant.	2 minutes.
Secondary	Sex	Participant's sex will be registered	2 minutes.
Secondary	Diagnosis of respiratory pathology	Participant's diagnosis will be registered.	2 minutes.