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RECRUITING
NCT05784740
NA

Precision Exercise to Improve Outcomes in Sepsis

Sponsor: University of British Columbia

View on ClinicalTrials.gov

Summary

The goal of this interventional clinical research study is to assess the efficacy of a 12-week precision exercise training intervention to improve exercise tolerance in sepsis survivors. The main question it aims to answer is does a 12-week precision exercise training program improve constant load exercise time in sepsis survivors? Participants will: * Answer questionnaires related to patient reported outcomes and give a blood sample * Perform a constant load exercise test * Complete 12-weeks (3 x per week, 36 session in total) of precision exercise training consisting of individualized, nonlinear periodized strength and aerobic exercise training. Researchers will compare the exercise group to an attention control group of sepsis survivors who do not receive exercise training but instead undergo usual care procedures and receive general lifestyle advice 1x per week.

Official title: Precision Exercise to Improve Patient Outcomes in Sepsis Survivors: PRECISE Study

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2023-04-17

Completion Date

2025-08

Last Updated

2024-12-18

Healthy Volunteers

No

Conditions

Interventions

OTHER

12-week precision exercise training

The 12-week exercise intervention will consist of both aerobic and strength exercise training performed 3x per week using an individualized and nonlinear periodized approach.

Locations (1)

St. Paul's Hospital - Centre for Heart Lung Innovation

Vancouver, British Columbia, Canada