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

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

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04703478

Enrollment

Registered

2021-01-11

Start date

2021-01-20

Completion date

2021-04-20

Last updated

2021-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Keywords

respiration disorders, telerehabilitation, breathing exercises, complications

Brief 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.

Interventions

OTHERBreathing 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.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
Rating of perceived exertion (Borg Scale)	10 minutes.	Scale from 1-10 points. Where number 1 means very light activity and 10, represents an extreme intensity of activity.
Level of satisfaction and acceptability.	20 minutes.	A Likert-type scale will be used. 1-Not Satisfied to 5-Extremely satisfied.
St. George's Respiratory Questionnaire, SGRQ	40 minutes.	scale from 0-100 points.Where higher scores mean worse outcomes.

Secondary

Measure	Time frame	Description
Age	2 minutes.	The date of birth will be registered in order to calculate the age of the participant.
Sex	2 minutes.	Participant's sex will be registered
Diagnosis of respiratory pathology	2 minutes.	Participant's diagnosis will be registered.

Countries

Spain

Contacts

Primary ContactBeatriz M Bermejo-Gil, Prof.

beatriz.bermejo@usal.es+34 622 289 468

Backup ContactRocio Llamas-Ramos, Dr.

rociollamas@usal.es+34 657 854 188

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026