Efficacy of smartphone application based rehabilitations in patients with chronic respiratory or cardiovascular disease

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008026

Enrollment

182

Registered

2022-12-23

Start date

2023-04-01

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

None listed

Interventions

Others : The rehabilitation program will be provided for 12 weeks through the provision of rehabilitation exercise video and intervention through a smartphone application to patients suffering from ch

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Obstructive pulmonary disease, bronchiectasis, restrictive pulmonary disease - Chronic respiratory disease (obstructive pulmonary disease, - Bronchiectasis, - Restrictive pulmonary disease with dyspnea of mMRC 1 or higher is intended for patients. - Coronary artery disease, angina pectoris, myocardial infarction, heart failure, * Chronic respiratory disease is based on the following criteria. * Obstructive pulmonary disease (chronic obstructive pulmonary disease, asthma, etc.): FEV1/FVC < 0.7 or FEV1 < 80% of the normal predicted value * Bronchiectasis: bronchiectasis confirmed in one or more lung lobes on chest CT * Restrictive lung disease (interstitial lung disease, etc.): FVC or DLCO < 80% of the normal predicted value * The subjects of cardiac rehabilitation are patients with coronary artery disease (angina pectoris, myocardial infarction) and heart failure with NYHA 2 or higher dyspnea. * Coronary artery disease: Patients who underwent reperfusion or surgery for angina pectoris or myocardial infarction * Heart failure: Patients being treated for left ventricular insufficiency (LVEF < 50%)

Exclusion criteria

Exclusion criteria: - Patients who have been hospitalized due to worsening of the disease within the last 4 weeks - Patients unable to perform the rehabilitation program provided by the app - Patients who are not suitable for participation in the study according to the judgment of the researcher - Patients who refused to consent to the study

Design outcomes

Primary

Measure	Time frame
Maximal oxygen consumption;Chronic obstructive pulmonary disease (COPD) assessment Test (CAT) ;Korean Health-related Quality of Life Instrument with 8 Items (HINT-8)	—

Secondary

Measure	Time frame
EuroQol 5-dimension 5-level;hand grip strength;limb muscle mass;dyspnea symptom	—

Countries

Korea, Republic of

Contacts

Public ContactChiwook Chung

Asan Medical Center

sawadax@naver.com+82-2-3010-0981

Outcome results