Precision Exercise to Improve Outcomes in Sepsis
Recruiting
N/A
Interventional Study
Sepsis
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 19 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 32 (estimated)
- Sponsor
- University of British Columbia · Other
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About This Trial
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 r…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Signed informed consent
* At least 19 years of age
* ≥60 days prior to study enrollment, known or suspected infection that includes at least two of the following clinical criteria that together constitute a new bedside clinical score termed quickSOFA (qSOFA): respiratory rate …
Contacts