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Elucidation of the effects of asynchronous remote exercise therapy on patients with chronic respiratory diseases

A prospective intervention study to clarify the effects of asynchronous remote exercise therapy for patients with chronic respiratory diseases - ReMOTE-CRD study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000058987
Enrollment
40
Registered
2025-10-01
Start date
2025-11-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chronic respiratory diseases

Interventions

In the intervention group, exercise therapy that can be performed at home, such as aerobic exercise and muscle strengthening exercises, will be prescribed by Recaval and instructed to the patients. Pa

Sponsors

SBC Tokyo Medical University
Lead Sponsor
Toho University Medical Center Omori Hospital, Kanamecho Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with COPD or IIPs and currently receiving outpatient care at the Department of Respiratory Medicine at Toyo University Medical Center Oomori Hospital or Yokocho Hospital 2.Patients aged 40 years or older at the time of consent acquisition 3.Patients who are able to walk independently 4.Patients whom a physician determines are capable of undergoing accurate pulmonary function tests and walking tests 5.Patients whose condition is stable and have not undergone any changes in treatment for over three months 6.Individuals who own a smartphone, tablet, or computer and are deemed capable of using this service 7.Patients who have received adequate explanation of the study content and have provided written informed consent 8.Patients currently enrolled in or who have completed an outpatient rehabilitation program, with stable symptoms, and who do not have an outpatient rehabilitation program scheduled during the course of this trial

Exclusion criteria

Exclusion criteria: 1.Patients with severe orthopedic or central nervous system disorders requiring assistance in daily living 2.Patients with a history of hospitalization within the past 6 months due to worsening of the underlying disease 3.Patients with unstable heart disease 4.Other patients for whom participation in this clinical study may compromise patient safety, or patients for whom compliance with the clinical study protocol is deemed difficult.

Design outcomes

Primary

MeasureTime frame
6-minute walking distance

Secondary

MeasureTime frame
6-minute walk test, quadriceps muscle strength, grip strength, dyspnea, health-related quality of life, activities of daily living, anxiety and depression, satisfaction survey, pulmonary function tests

Countries

Japan

Contacts

Public ContactSoh Imamura

SBC Tokyo Medical University Department of Physical Therapy, Faculty of Health Care Sciences

s-imamura@sbctmu.ac.jp047-382-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026