ClinicalTrials.gg
CompletedNCT06804317Updated Feb 3, 2025

Effectiveness of a Supervised Multicomponent Exercise-Based Telerehabilitation Intervention on Physical Performance in Older Patients with Multiple Chronic Conditions in Colombia

An interventional study of telerehabilitation in Non Communicable Chronic Diseases, sponsored by Fundacion Universitaria Maria Cano. Completed at 1 site in Colombia. Open to participants aged 60 Years to 100 Years. Per ClinicalTrials.gov, last updated 2025-02-03.

Sponsored by Fundacion Universitaria Maria Cano · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Feb 2024, registered Jan 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
41
Allocation
Not applicable
Ages
60 Years to 100 Years
Sex
All
01

Study summary

Currently, the older adult population faces an increase in the prevalence of cardiopulmonary diseases, which negatively impact their quality of life by limiting their ability to perform daily activities and affecting their physical and emotional well-being. In particular, cardiovascular and respiratory diseases are among the leading causes of morbidity and mortality among older adults in Colombia. Despite advances in pharmacological treatment and medical care, physical rehabilitation remains an essential component in the management of these diseases, with physical exercise serving as one of its fundamental pillars. However, access to physical rehabilitation programs for the older adult population, particularly in rural or hard-to-reach areas, continues to pose a significant challenge. Telemedicine and Information and Communication Technologies (ICT) have emerged as viable solutions to overcome this barrier, enabling the remote prescription and monitoring of physical exercises, facilitating the inclusion of more patients in rehabilitation programs, and improving their quality of life. Therefore, this study aims to evaluate the effectiveness of a multicomponent ICT-mediated intervention in terms of improving physical condition, reducing frailty, adherence, satisfaction, and quality of life in older adults with cardiopulmonary diseases.

02

Conditions studied

  • Non Communicable Chronic Diseases

Keywords

  • Exercise Therapy
  • elderly
  • telerehabilitation
03

In context

Noncommunicable Diseases

144 studies on the registry are indexed under Noncommunicable Diseases; 55 are open to participants now.

This study's enrollment of 41 is below the median of 478 across 95 interventional studies indexed under Noncommunicable Diseases.

Browse Noncommunicable Diseases studies →

Lead sponsor

Fundacion Universitaria Maria Cano is the lead sponsor of 7 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosis of a non-communicable disease.
  • Ability to communicate verbally or in writing.
  • Stable disease status confirmed by clinical history.
  • Condition present for at least three months to qualify as chronic.
  • For patients with type II diabetes mellitus: glucose levels below 200 mg/dL during tele-rehabilitation sessions.

Exclusion criteria

Exclusion Criteria

  • Requirement for assistance with walking.
  • History of disease exacerbation within the past six months.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
41 participants (actual)

Study arms

  • Experimental
    NCD´s Telerehabilitation

    41 participants enrolled in a tele-rehabilitation program with Exercise-based interventions conducted twice weekly for three months via videoconferencing on Microsoft Teams

    Other: telerehabilitation

Interventions

  • Othertelerehabilitation

    Exercise-based interventions were conducted twice weekly for three months via videoconferencing on Microsoft Teams. The program included various components: Aerobic and strength training, Flexibility, Balance and coordination

06

What researchers measure

Primary outcomes

  1. Short Physical Performance Battery

    This battery includes tests for usual walking speed over 4 meters, five-chair stands, and balance. Each task receives a score (0-4) based on the time required to perform five sit-to-stand repetitions, standing balance, and walking speed over 4 meters. The total score (0-12) is calculated by summing individual scores, with higher scores indicating better lower-body function.

    Time frame: Baseline and at 1 month postest

Secondary outcomes

  1. Six-minute walk test

    Conducted on a straight, level, hard surface, ideally 30 meters long, with a minimum acceptable length of 20 meters. The track was marked every 3 meters, with cones at the ends and bright tape at the start. Variables recorded included meters (m), which represent the total distance covered by the individual during the six-minute period.

    Time frame: Baseline and at 1 month postest

07

Study locations

1 site
  • Fundación universitaria María Cano
    Medellín, Colombia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06804317
Lead sponsor
Fundacion Universitaria Maria Cano
Responsible party
Catalina Lopera Muñetón (clinical professor, Fundacion Universitaria Maria Cano) — Principal investigator
First posted
Feb 3, 2025
Start date
Feb 1, 2024
Primary completion
Nov 14, 2024
Completion
Dec 30, 2024
Last update
Feb 3, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion