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Effects of early rehabilitation intervention for general hospital inpatients on ADL at discharge, length of stay, and medical costs: a cluster randomized controlled trial

Effects of early rehabilitation intervention for general hospital inpatients on ADL at discharge, length of stay, and medical costs: a cluster randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030240003
Enrollment
126
Registered
2024-04-03
Start date
2024-04-01
Completion date
Unknown
Last updated
2025-07-18

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

Conditions

Disuse syndrome Disuse syndrome

Interventions

Comprehensive rehabilitation conducted twice a day (morning and afternoon) for approximately 20 minutes each time by physical therapists, occupational therapists, and speech therapists who work at Tok
Rehabilitation

Sponsors

Kobayashi Daiki
Lead Sponsor
Ito Hiroshi
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who meet the following criteria are eligible. 1) Persons who are 70 years of age or older at the time of obtaining consent 2) Persons hospitalized from home 3) Those who have received sufficient explanation and informed written consent of the research subject or his or her family to participate in this research.

Exclusion criteria

Exclusion criteria: 1) Persons whose hospitalization period is estimated to be less than 14 days 2) Persons admitted to intensive care unit 3) Persons who were expected to die at the time of admission and received best supportive care. 4) Persons with uncontrolled arrhythmia 5) Those who have had acute myocardial infarction within 30 days before hospitalization 6) Persons with acute pulmonary embolism 7) Those who have undergone surgical surgery under general anesthesia within 30 days before hospitalization 8) Those who have suffered a limb fracture within 30 days before hospitalization. 9) Any other person who is judged by the research physician to be inappropriate as a research subject.

Design outcomes

Primary

MeasureTime frame
Barthel index at discharge

Secondary

MeasureTime frame
Length of hospital stay, medical expenses during hospitalization, 30-day readmission rate, 30-day mortality rate, return-to-home rate

Contacts

Public ContactDaiki Kobayashi

Tokyo Medical University Ibaraki Medical Center

daikoba@tokyo-med.ac.jp+81-298871161

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Feb 4, 2026