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CardioSafe+: A Platform for Telerehabilitation and Monitoring of Patients With Heart Problems

CardioSafe Plus: A Platform for Telerehabilitation and Monitoring of Patients With Heart Problems.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05865158
Acronym
CardioSafe+
Enrollment
60
Registered
2023-05-18
Start date
2022-09-20
Completion date
2024-06-22
Last updated
2023-11-09

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

Conditions

Cardiovascular Diseases

Brief summary

The use of telerehabilitation seems to be effective in managing complications after suffering a cardiovascular pathology. The use of the CardioSafe+ digital platform is suggested for the management of these complications. For this reason, an intervention will be carried out to determine the effectiveness of this platform. A total of 60 participants will be recruited to carry out a home-exercise intervention through CardioSafe+ for 6 weeks. Maximun respiratory pressures, exertion capacity, and subjective sensation of exertion will be assessed.

Detailed description

This intervention seeks to determine the effectiveness of the CardioSafe+ digital platform in aiding individuals recovering from cardiovascular pathologies. By involving a group of 60 participants in a structured six-week home-exercise program using the CardioSafe+ platform, the objective is to measure and evaluate various factors related to their physical well-being and recovery. Key components to be evaluated include: Maximal Respiratory Pressures: This involves measuring the maximum force generated during inspiration and expiration, which can indicate respiratory muscle strength and function. Exertion Capacity: The assessment aims to gauge the participants' ability to engage in physical activities, potentially reflecting improvements in overall cardiovascular fitness and endurance. Subjective Sensation of Exertion: This component involves understanding how the participants perceive and rate their own exertion during exercises, contributing to insights about their subjective experience and effort perception. The intervention's objective is to collect data on these parameters before and after the six-week exercise program utilizing the CardioSafe+ digital platform. This data will help determine the effectiveness of the platform in aiding individuals recovering from cardiovascular pathologies and could provide valuable insights for further implementing tele-rehabilitation in managing such health complications.

Interventions

Home-based exercises proposed through the CardioSafe+ platform, guided by therapists specialized in cardiovascular disorders, who will try to adapt the sessions to each participant.

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* People who present a cardiovascular pathology with more than one year of evolution. * To be in a stable medical situation. * To have access to technological resources and knowledge for their use.

Exclusion criteria

* People who present any contraindication established for carrying out physical activity. * People who present insufficient capacity to understand and obey the instructions offered by the researchers, both in the evaluation and in the intervention. * People who have a cardiac pathology with obvious fluctuations in the course of the disease. * The presence of an acute episode of the disease during the intervention period.

Design outcomes

Primary

MeasureTime frameDescription
Maximum inspiratory pressure by spirometry6 weeksValue of the maximum inspiratory capacity in mm of H2O.
Maximum expiratory pressure by spirometry6 weeksValue of the maximum expiratory capacity in mm of H2O.
Borg Rating of Perceived Exertion Scale6 weeksScale of perceived subjective effort in which it is valued with a score of 0 to 10, subjectively. Started from 0 where your breathing is causing you no difficulty at all and progresses through to number 10 where your breathing difficulty is maximal.
2 minute stationary walk test6 weeksEffort test in which the participant is asked to lift their knees for 2 minutes and the number of times is counted. Based on that number, the percentile in which the person is based on their age and sex is calculated.

Countries

Spain

Contacts

Primary ContactBeatriz María Bermejo Gil, Dr
beatriz.bermejo@usal.es622289468
Backup ContactFátima Pérez Robledo
fatima_pr@usal.es622289468

Outcome results

None listed

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