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Evaluation of the Effectiveness, Safety, and Cost of a Smart Hospital System for Patients With Chronic Obstructive Pulmonary Disease

Yonsei University logo

Yonsei University

Status

Enrolling

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Behavioral: Delayed application of the Smart Homespital system after 3 months
Behavioral: Immediate application of the Smart Homespital system

Study type

Interventional

Funder types

Other

Identifiers

NCT06601777
4-2024-0299

Details and patient eligibility

About

This study aims to analyze the effectiveness/safety/cost of the Smart Homespital system that provides a service that allows patients with Chronic Obstructive Pulmonary Disease to easily access and use biosignals generated using biosignal collection medical equipment at home.

Enrollment

198 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients diagnosed with COPD who meet the following pulmonary function test results:

  1. Pre FEV1 < 80% **or**
  2. Pre FVC < 80% **or**
  3. DLCO < 60%

Exclusion criteria

  1. Patients who do not agree to participate in the study.
  2. Patients who fail to use the medical device equipment.
  3. Patients where tracking during the study period is expected to be impossible.
  4. Patients who have difficulty communicating verbally.
  5. Patients who are bedridden or unable to exercise at all due to severe cardiorespiratory dysfunction.
  6. Patients receiving hospital-centered rehabilitation treatment during the study period.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

198 participants in 2 patient groups

intervention group
Experimental group
Description:
The Smart Homespital system can be applied for the first 3 months (12 weeks), and then the primary and secondary variables will be evaluated at 3, 6, 9months.
Treatment:
Behavioral: Immediate application of the Smart Homespital system
attention-waitlist control group
Experimental group
Description:
The waiting list-control group will receive general medical services for the first 3 months and will receive the Smart Homespital system for 3-6 months. Primary and secondary variables will be evaluated between 3, 6, and 9 months.
Treatment:
Behavioral: Delayed application of the Smart Homespital system after 3 months

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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