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An Intelligent Cardiopulmonary Rehabilitative System on Cardiopulmonary Fitness

An Intelligent Cardiopulmonary Rehabilitative System on Cardiopulmonary Fitness

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04662307
Enrollment
10
Registered
2020-12-10
Start date
2020-12-15
Completion date
2023-01-15
Last updated
2022-05-11

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

Conditions

Lifestyle, Sedentary

Keywords

cardiac rehabilitation, cardiorespiratory fitness, aerobic exercise, endurance training

Brief summary

Contemporary cardiopulmonary rehabilitation programs often utilize cycling ergometer, involving one-on-one heart rate monitoring by physiotherapists to ensure that patients reach the target training intensity during training sessions. However, the process is frequently described as monotonous and boring, resulting in early fatigue of therapists and patients as well as poor compliance, leading to undertraining and suboptimal outcomes. This study aims to test the feasibility of the Intelligent Cardiopulmonary Training System (ICRS) and a novel indicator of measuring the adherence to training intensity. The ICRS was developed with the idea to provide machine-based supervision on the user's heart rate during training. It provides moderate-intensity continuous training with a cycling ergometer. This system automatically adjusts the paddling resistance according to the user's real-time heart rate, and helps to improve the user's adherence to pre-determined training intensity without trainer's watch. The automation of intensity adjustment has its potential for conditions in which supervision is not feasible.

Interventions

DEVICEIntelligent cardiopulmonary rehabilitation system (ICRS)

Participants are required to wear a wristband heart rate monitor and exercise on a cycling ergometer-based ICRS for 30 minutes (5 minute of warm-up, 20 minutes of training followed by 5 minutes of cooldown). The target intensity for the 20-min training period is set at 60%\ 80% HRR determined in the pretest of cardiopulmonary exercise test.

Sponsors

Taipei Medical University WanFang Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A small group of healthy subjects with sedentary lifestyle is recruited to validate the ICRS. They receive training with ICRS three sessions a week, for a total of 12 sessions. The outcome assessments are performed before and after the training.

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

1\. Sedentary healthy people

Exclusion criteria

* Patients whose heart rate can not be used as the indicator of training intensity (eg, ar-rhythmia, atrial fibrillation, beta-blockers users) * With any reason that the patient is not suitable to undergo * Patients who are unable to do cycling due to musculoskeletal problems * Patients who can not follow the instruction of trainers due to cognitive or emotional-problems. * Patients whose medical condition is not unstable.

Design outcomes

Primary

MeasureTime frameDescription
Peak oxygen consumption (VO2-peak)4 weeksPeak oxygen consumption is measured by cardiopulmonary test.

Secondary

MeasureTime frameDescription
Peak workload4 weeksPeak workload is measured by cardiopulmonary exercise test
percentage of time (%time) within the pre-determined target heart rate4 weeksThe ICRS outputs the heart rate-time plots and calculated the %time for each session

Countries

Taiwan

Outcome results

None listed

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