NCT04575220

Adaptive Home Based Pulmonary Tele-exercise

Pilot Study of Adaptive Home Based Pulmonary Tele-exercise (AHTE)
Gerald Supinski·ClinicalTrials.gov·otherRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Rehabilitation
Drug/Device/Intervention
12 weeks of bicycle exercise
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
Gerald Supinski
Funder
University of Kentucky
Location
Lexington, United States of America
Timeline & enrollment
Phase
N/A
Start date
Oct 20, 2020
End date
Dec 01, 2022
Enrollment
12 participants
Primary outcome

80% work rate test

Summary

The goal of this pilot study is to determine if a home based bicycle exercise program can
 significantly improve the exercise tolerance and well being of pulmonary outpatients. The
 investigators will use a computer based monitoring system to allow us to speak with
 participants, view participants, and track patient bicycle activity (speed, duration of
 exercise, rate of work) during exercise sessions. The investigators plan to have participants
 perform three telemonitored exercise sessions per week for 12 weeks as part of this program.
 The investigators will assess exercise performance on the bicycle, called a work rate test,
 at the beginning of the program and then again at 6 weeks and 12 weeks into the program to
 determine if the program can produce a clinically significant improvement in work rate test
 performance (i.e. a greater than 1.15 minute increase in exercise duration at an 80% work
 rate). The investigators will also assess participant CRQ, SPPB scores and SF36 scores
 (indices of patient well being) at baseline, at 6 weeks, and at 12 weeks, to determine if the
 exercise program elicits an increase in these indices.

ICD-10 classifications
Care involving use of rehabilitation proceduresDrug rehabilitationCare involving use of other rehabilitation proceduresCare involving use of rehabilitation procedure, unspecifiedPersonal history of rehabilitation measures
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04575220
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT04575220 through Pure Global AI's free database. This phase not specified trial is sponsored by Gerald Supinski and is currently Recruiting. The study focuses on Rehabilitation. Target enrollment is 12 participants.

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