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Activity on Prescription to Promote Physical Activity in Hospitalized Patients

H

Heidelberg University

Status

Unknown

Conditions

Physical Activity

Treatments

Procedure: "Prescription for Activity" and individual instructions
Other: "Prescription for Activity", without instructions
Other: usual physiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT01622829
S-602/2011

Details and patient eligibility

About

This study tries to improve patient's activity by a "Prescription for Activity" led by physiotherapists in secondary health care setting.

Three groups are compared in regard to their increase of physical activity.

Enrollment

120 estimated patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 40-75 years
  • self-dependent
  • walk around at home alone
  • German-speaking
  • Ability to read and write
  • Life expectancy > 6 months
  • Stable disease process expected for the next 6 months
  • Time spend in hospital: > 3 days, < 4 weeks

Exclusion criteria

  • Patients suffering from dementia
  • Planned participation in rehabilitation
  • severe functional limitations that precluded any increase in physical activity
  • not living independently

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

120 participants in 3 patient groups

group1
Experimental group
Description:
Usual Physiotherapy, additional: "Prescription for Activity" with a structured fitness program and individual instructions to become more active in the daily living situation
Treatment:
Procedure: "Prescription for Activity" and individual instructions
group 2
Experimental group
Description:
usual Physiotherapy , additional: "Prescription for Activity" without instructions
Treatment:
Other: "Prescription for Activity", without instructions
group 3
No Intervention group
Description:
control, usual physiotherapy
Treatment:
Other: usual physiotherapy

Trial contacts and locations

1

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Central trial contact

Peter Beartsch, MD; Stephanie Intorp

Data sourced from clinicaltrials.gov

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