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Physical Training During Hospital Admission With Community-Acquired Pneumonia

Physical Training During Hospital Admission With Community-Acquired Pneumonia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04094636
Enrollment
210
Registered
2019-09-19
Start date
2019-04-01
Completion date
2022-10-01
Last updated
2022-02-15

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

Conditions

Community-acquired Pneumonia

Keywords

Physical training

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALIn-bed cycling

Patients will daily perform 30 min of supervised in-bed cycling

Patients will daily perform 30 min of supervised physical training with exercises from the exercise booklet

Sponsors

Nordsjaellands Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Length of hospital stayFrom admission until discharge (an average of 5 days)Number of stays in hospital

Secondary

MeasureTime frameDescription
Changes in total fat-free massDay 1, day 5, discharge, 1- and 3-months from dischargeBioelectrical impedance analysis
Muscle strengthAt day 1, day 5, discharge, 1- and 3-months after dischargeHand grip strength test
Functional abilityDay 1, day 5, discharge, 1- and 3-months after discharge30-sec chair stand test
Systemic inflammationDaily during admission (day 0 to 5), 1- and 3-months after dischargePro- and anti-inflammatory cytokine concentrations measured in pg/ml (IL-6, IL-8, IL-18, IL-1a, IL-10, TNF-alpha)
Physical activity monitoringDuring admission (up to 7 days), 7 days from discharge, 7 days from 1- and 3 months follow-upAX3 accelerometers
Readmissions Number of readmissions3-months from dischargeTime-to-event within 3-months from discharge
Mortality6-months from dischargeTime-to-event within 6-months from discharge
Changes in total lean massDay 1, day 5, discharge, 1- and 3-months from dischargeDual-energy x-ray absorptiometry scans
Changes in total fat massDay 1, day 5, discharge, 1- and 3-months from dischargeDual-energy x-ray absorptiometry scans
Health-related quality of lifeDay 1, discharge, 1-, 3- and 6-months from dischargeScoring from -0.624 to 1.000 on the 5-level EQ-5D version (EQ-5D-5L) questionnaire (Danish version), with higher score indicating better health-related quality of life
Activities of daily livingDay 1, discharge, 1 month from discharge and 3 months from dischargeScoring from 0 to 100 on the Barthel Index for Activities of Daily Living (ADL) with higher score indicating greater independence.

Other

MeasureTime frameDescription
Scoring on the Charlson Comorbidity Index to predict 10-year survivalDay 1Scale ranges from 0 to 33 points to predict he 10-year mortality for patients with a range of comorbid conditions
HbA1cDay 1, 1- and 3-months after dischargeTo assess the average blood glucose levels over the previous 3 months
Glucose metabolismDay 1, 1- and 3-months from dischargeBlood samples drawn during an oral glucose tolerance test
Self-reported physical activity (PA) levelAnswered on day 1, 1-, 3- and 6 months after discharge3 groups of PA level (high, medium, low) are established based on the scoring of the international physical activity questionnaire (IPAQ). * High PA level: Vigorous-intensity activity on at least 3 days and accumulating a minimum of 1500 MET-minutes/week OR 7 or more days of any combination of walking, moderate-intensity or vigorous intensity activities achieving a minimum of 3000 MET-minutes/week * Medium PA level: 3 or more days of vigorous-activity of at least 20 minutes/day OR 5 or more days of moderate-intensity activity or walking of at least 30 minutes/day OR 5 or more days of any combination of walking, moderate-intensity or vigorous-intensity activities achieving a minimum of 600 MET-min/week. * Low PA Level: No activity is reported OR some activity is reported but not enough to meet criteria for high or medium PA level group.

Countries

Denmark

Contacts

Primary ContactCamilla Ryrsø, MSc
camilla.koch.ryrsoe.01@regionh.dk+4548293261

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026