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New treatment option for Sepsis
Official title Precision Exercise to Improve Outcomes in Sepsis
ClinicalTrials.gov ID: NCT05784740
What this study is testing
- What it's testing
- 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?
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 19 and older
You may be able to join if
- 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...
- Cardiorespiratory fitness \<80% of age and sex-predicted norms
- Can commit to attending 3 exercise sessions a week for 12-weeks
You likely can't join if
- Unable to provide informed consent
- On supplemental oxygen
- Known previous cardiac or cerebral vascular events in the past 90 days
- Diabetes
- Autoimmune diseases or on daily immunomodulatory drugs
- Obstructive sleep apnea
See the full eligibility 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...
- Cardiorespiratory fitness \<80% of age and sex-predicted norms
- Can commit to attending 3 exercise sessions a week for 12-weeks
- Unable to provide informed consent
- On supplemental oxygen
- Known previous cardiac or cerebral vascular events in the past 90 days
- Diabetes
- Autoimmune diseases or on daily immunomodulatory drugs
- Obstructive sleep apnea
- Uncontrolled hypertension
- Known pregnancy/ intending to get pregnant within 28 days of enrolling in the study or breastfeeding
- Desaturation during exercise SpO2\<85%
- Cardiovascular contraindication or musculoskeletal limitations to exercise as assessed during the cardiopulmonary exercise test
The study team makes the final eligibility decision.
Where it's taking place
- Vancouver, British Columbia, Canada
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 19 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Vancouver, British Columbia, Canada. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.