Functional Characterization of CD8+ T Cells After Supramaximal Exercise
Effekten av högintensiv träning på Vita Blodkroppar, Med Speciellt Fokus på Funktion Kopplad Till Att bekämpa Cancerceller
1 other identifier
interventional
7
1 country
1
Brief Summary
Healthy human subjects perform supramaximal exercise with venous blood samples obtained before and up to 60 minutes after the exercise bout.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 31, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 22, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 14, 2024
CompletedFirst Submitted
Initial submission to the registry
June 18, 2024
CompletedFirst Posted
Study publicly available on registry
July 3, 2024
CompletedJuly 3, 2024
June 1, 2024
9 months
June 18, 2024
June 28, 2024
Conditions
Outcome Measures
Primary Outcomes (3)
CD8 T cell absolute nr after exercise
CD8 nr
Before, directly after, 60 minutes after exercise
CD8 T cell cytotoxicity against cancer cells
CD8 T cell lysis of cancer cells
Cryopreserved CD8 cells from Day 1 and Day 8 of the experiment, obtained before and after exercise
CD8 T cell pheontype after exercise
Flow cytometry analysis of CD8 T cells
Before, directly after, 30 minutes and 60 minutes after exercise
Study Arms (1)
Exercise
EXPERIMENTALHealthy human subjects performing 3 x 30 seconds of supramaximal exercise with blood obtained before and up to 60 minutes after the exercise bout
Interventions
Eligibility Criteria
You may qualify if:
- Be used to physical exercise and be able to perform strenous exercise Be able to attend the experimental procedure for the 90 minute duration of the study
You may not qualify if:
- Smoking Pregnant Have any medical condition requiring medical treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Karolinska Sjukhuset Huddinge
Huddinge, Stockholm County, Sweden
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Helene Rundqvist, PhD
Karolinska Institutet
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
June 18, 2024
First Posted
July 3, 2024
Study Start
March 31, 2023
Primary Completion
December 22, 2023
Study Completion
February 14, 2024
Last Updated
July 3, 2024
Record last verified: 2024-06
Data Sharing
- IPD Sharing
- Will not share