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Clinical Trials/JPRN-UMIN000053176
JPRN-UMIN000053176
Not yet recruiting
未知

Effectiveness of home-based exercise therapy using remotely controlled cycling exercise system in patients with mild cognitive impairment due to non-Alzheimer's disease. - Effectiveness of remotely controlled cycling exercise system in patients with mild cognitive impairment due to non-Alzheimer's disease.

Osaka University0 sites45 target enrollmentJanuary 15, 2024

Overview

Phase
未知
Intervention
Not specified
Conditions
Mild cognitive impairment due to non-Alzheimer&#39
Sponsor
Osaka University
Enrollment
45
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 15, 2024
End Date
September 30, 2026
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Patients who do not have or cannot establish a reliable Internet environment at home (2\) Patients for whom exercise therapy is considered contraindicated (3\) Patients who have difficulty pedaling the exercise bike used for exercise therapy due to other diseases or pain (4\) Patients who have difficulty operating the application due to visual or hearing impairment (5\) Patients who have had hypotension, fatal arrhythmia, or other adverse events during rehabilitation, exercise stress tests, or exercise therapy (6\) Patients with acute myocardial infarction leaving untreated significant (\>75%) coronary artery stenosis in \[AHA classification: \#1,2,3,5,6,7,11,13] in the major three branches (7\) Patients with end\-stage heart failure (8\) Patients with evidence of residual myocardial ischemia (9\) Patients with poorly controlled heart failure (10\) Patients after implantation of left ventricular assist device (11\) Patients with a pacemaker, ICD, or implantable cardiac monitor (12\) Patients whose prognosis is expected to be within 6 months (13\) Patients who have participated in other clinical trials or clinical studies involving interventions within the past 12 weeks of obtaining consent (14\) Patients who are judged by the investigators to be incapable of properly understanding the significance of the research and complying with the compliance requirements.

Outcomes

Primary Outcomes

Not specified

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