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Physical Training During Hospital Admission With Community-Acquired Pneumonia

N

Nordsjaellands Hospital

Status

Unknown

Conditions

Community-acquired Pneumonia

Treatments

Behavioral: In-bed cycling
Behavioral: Exercise booklet

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to assess the effect of standard usual care combined with daily supervised physical training during hospitalization with community-acquired pneumonia (CAP) compared to standard usual care alnone.

Full description

Community-acuired pneumonia (CAP) is a leading cause of hospitalization worldwide. Despite increased focus on mobilization, hospitalization is associated with bed rest. Bed rest with low levels of physical activity leads to functional deline as well as increased risk of complications.

This study is a randomized controlled trial, which investigates the effect of standard usual care combined with daily supervised physical training in patients hospitalized with CAP compared to standard usual care alone.

Enrollment

210 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients 18 years of age or older admitted to hospital with CAP defined as a new infiltrate on chest X-ray/CT and minimum one of the following symptoms: temperature <35˚C or ≥38˚C, cough, pleuritic chest pain, dyspnea, or focal chest signs on auscultation.
  • Patients should have an expected admission length of ≥72 hours.
  • Patients should be able to move their legs.

Exclusion criteria

  • Patients unable to give written consent.
  • Hospital admission within the last 14 days.
  • Severe immunosuppression (cancer chemotherapy ≤28 days, neutropenia ≤1000 cells/μL, ≥20 mg prednisolone-equivalent/day >14 days or other immunosuppressive drugs, HIV infection, former transplant).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

210 participants in 3 patient groups

No intervention: Control
No Intervention group
Description:
Control group
In-bed cycling
Experimental group
Description:
Supervised in-bed cycling
Treatment:
Behavioral: In-bed cycling
Exercise booklet
Experimental group
Description:
Supervised physical training with exercises from exercise booklet
Treatment:
Behavioral: Exercise booklet

Trial contacts and locations

1

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Central trial contact

Camilla Ryrsø, MSc

Data sourced from clinicaltrials.gov

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