NCT06884644

Brief Summary

During the exercise intervention "Death by Squats", which compasses body weight squats until maximum exertion, 25-30 subjects shall be tested for heart rate, the oxygen saturation of the vastus medialis and the triceps, resting and at maximum exertion blood lactate, as well as the rate of perceived exertion on the borg scale. At the end, all should indicate their primary reason for stopping (local fatigue, systemic fatigue, time constraints, motivational deficit).

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 8, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

February 8, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 19, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

March 19, 2025

Status Verified

March 1, 2025

Enrollment Period

10 months

First QC Date

February 8, 2025

Last Update Submit

March 18, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Local and systemic SmO2 curve

    From the start of the exercise intervention until individual exhaustion (expected between 15 to 30 minutes), with SmO₂ continuously recorded during exercise and final measurement taken immediately upon exhaustion.

Secondary Outcomes (1)

  • Type of sports practiced

    Questionnaire administered within 5 minutes after test completion to assess type of sports practiced.

Other Outcomes (2)

  • Anthropometric parameters will be assessed

    Anthropometric measurements will be taken immediately after the completion of the exercise intervention (expected between 15 to 30 minutes after the start of exercise).

  • Blood lactate concentration at rest and post-exercise

    At rest (prior to exercise) and immediately upon individual exhaustion (expected between 15 to 30 minutes after the start of exercise). Additional post-exercise measurements at 2, 5, and 10 minutes if applicable.

Study Arms (1)

Death by Airsquat Exercise

All participants follow the exercise protocol, based on the "every minute on the minute" principle: Starting off with 10 body weight squats in the first minute (after completion, the remaining seconds can be always be used as a break). In minute two, 12 squats have to be completed. In minute three, 14 squats, and so forth. Until maximum exertion is reached and/or until the number of squats within 60 seconds can not be increased further. Every individual stops at his/her performance limit

Diagnostic Test: Death by Airsquat

Interventions

Death by AirsquatDIAGNOSTIC_TEST

Increasing number of squats have to be completed every minute (EMOM principle).

Death by Airsquat Exercise

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Male and female participants of 18 years and older, that are performing a CrossFit class with the EMOM workout "Death by Airsquat".

You may qualify if:

  • being moderately to severely physically active al least 2 hours/week (all types of sport are eligible)

You may not qualify if:

  • akute infections, musculoskeletal injuries
  • chronic cardiovascular or pulmonary diseases (in case of uncertainty, we recommend appraisal from medical personnel)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of the Bundeswehr Munich

Munich, Bavaria, 85577, Germany

RECRUITING

MeSH Terms

Conditions

Fatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Annette Schmidt, Prof

CONTACT

Jennifer Schlie, M.Sc.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
24 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr. Annette Schmidt

Study Record Dates

First Submitted

February 8, 2025

First Posted

March 19, 2025

Study Start

February 8, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

March 19, 2025

Record last verified: 2025-03

Locations