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The Preventing Functional Decline in Acutely Hospitalized Older Patients (PREV_FUNC) Study

NCT05366075 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 320

Last updated 2024-12-20

No results posted yet for this study

Summary

This study aims to examine 1) if multicomponent exercise interventions (including both mobility and strengthening exercises) have effects on physical function compared to usual care in older adults, and 2) if a comprehensive multicomponent exercise program is more effective than a simple multicomponent exercise program including only walking and rising from a chair.

Conditions

  • Hospitalization
  • Older Adults

Interventions

OTHER

Intervention 1 (simple exercise program)

Up to four sessions per day (total duration 20-30 minutes/day). Performed at the hospital on all weekdays from baseline until hospital discharge (around 1 week). At discharge, the participants will be encouraged to continue with the exercise program at home.

OTHER

Intervention 2 (comprehensive exercise program)

Two daily sessions (morning and afternoon) of 20 minutes' duration each. Performed at the hospital on all weekdays from baseline until hospital discharge (around 1 week).

Sponsors & Collaborators

  • Swedish Council for Working Life and Social Research

    collaborator OTHER

  • Center for Innovative Medicine

    collaborator UNKNOWN

  • Konung Gustaf V:s och Drottning Victorias Frimurarestiftelse

    collaborator UNKNOWN

  • Karolinska Institutet

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2025-06-30
Completion
2026-06-30

Countries

  • Sweden

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05366075 on ClinicalTrials.gov