The Effect of Exercise on Physical Function and Health in Older People After Discharge From Hospital "OLPADIS"

Recruiting

Phase N/A Results N/A

Trial Description

The aim of this study is to investigate the effect of a multi-component exercise program on physical function, physical activity and health-related quality of life (HRQOL) in older people recently discharged from hospital. The intervention consists of 32 group-based exercise sessions, performed twice a week. In addition the participants in the intervention group will be encouraged to perform an exercise program on their own, at least once weekly. The participants in the control group will be encouraged to exercise on their own, according to the World Health Organization (WHO) recommendations on physical activity for adults aged 65 and above.

Detailed Description

Older people who have been hospitalized often experience loss of function, increased risk of falls and reduced health-related quality of life (HRQOL) in the post-discharge period. The reason for this is the cumulative effect of illness, bedrest during hospital stay and inactivity after discharge. Previous research indicates that exercise therapy should be an integrated part of the post-hospital treatment to prevent or postpone this functional decline and improve HRQOL. Therefore, the investigators will conduct a randomized controlled trial to investigate the effect of a multi-component exercise program consisting of high intensity exercises on physical function, physical activity and HRQOL among older people living at home after discharge from hospital after treatment of an acute medical event.

Conditions

Interventions

  • Exercise Other
    Intervention Desc: A multi-component exercise program that consists of endurance training, progressive strength exercises and balance exercises.
    ARM 1: Kind: Experimental
    Label: Exercise
    Description: This group will perform a multi-component exercise program twice a week for 16 weeks. The multi-component exercise program consists of endurance training, progressive strength exercises and balance exercises. The intervention will be individualised, but performed in groups of four to ten patients. The participants are also expected to do exercises on their own, at least once weekly.

Trial Design

  • Allocation: Randomized
  • Masking: Single Blind (Outcomes Assessor)
  • Purpose: Health Services Research
  • Endpoint: Safety/Efficacy Study
  • Intervention: Parallel Assignment

Outcomes

Type Measure Time Frame Safety Issue
Primary Changes in physical function Baseline, 4 months and 8 months No
Secondary Berg Balance Scale Baseline, 4 months and 8 months No
Secondary Health-related quality of life (HRQOL) Baseline, 4 months and 8 months No
Secondary Physical Activity measured by the short form of the International Physical Activity Questionnaire (IPAQ-SF) Baseline, 4 months and 8 months No
Secondary Muscle mass Baseline, 4 months and 8 months No
Secondary Compliance to the intervention Eight months from baseline No
Secondary Feasibility of the intervention Four months from baseline No
Secondary Amount of home-help services received Baseline, 4 months and 8 months No
Secondary Handgrip strength Baseline, 4 months and 8 months No
Secondary Height Baseline No

Sponsors