The 10/7 HIIT Shock Cycle Study: Effectiveness of 10 HIIT Sessions in 7 Days
THESIS
1 other identifier
interventional
33
1 country
1
Brief Summary
A randomized, controlled trial to evaluate the effects of two versions of 10 high intensity interval trainings (HIIT) within a 7-day shock microcycle on endurance performance, well-being, health, stress and recovery in trained athletes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started Aug 2021
Typical duration for not_applicable healthy
1 active site
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
Study Start
First participant enrolled
August 15, 2021
CompletedFirst Submitted
Initial submission to the registry
September 6, 2021
CompletedFirst Posted
Study publicly available on registry
October 5, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedJanuary 31, 2024
January 1, 2024
1.4 years
September 6, 2021
January 30, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Endurance performance I
Change of maximal oxygen uptake (VO2max in ml/min/kg) compared to baseline and group
10 to 21 days (assessment is conducted once before the intervention and repeated three times afterwards, i.e. 3, 7 and 14 days after the completion of the intervention)
Endurance performance II
Change of peak performance (Ppeak in Watt) compared to baseline and group
10 to 21 days (assessment is conducted once before the intervention and repeated three times afterwards, i.e. 3, 7 and 14 days after the completion of the intervention)
Endurance performance III
Change of 5 kilometer time trial performance (in sec) compared to baseline and group
20 to 22 days (the assessment is conducted once before, and once after the intervention)
Endurance performance IV
Change of lactate threshold (in km/h) compared to baseline and group
10 to 21 days (assessment is conducted once before the intervention and repeated three times afterwards, i.e. 3, 7 and 14 days after the completion of the intervention)
Endurance performance V
Change of ventilatory thresholds (in km/h) compared to baseline and group
10 to 21 days (assessment is conducted once before the intervention and repeated three times afterwards, i.e. 3, 7 and 14 days after the completion of the intervention)
Endurance performance VI
Change of running economy (in ml/min/kg) compared to baseline and group
10 to 21 days (assessment is conducted once before the intervention and repeated three times afterwards, i.e. 3, 7 and 14 days after the completion of the intervention)
Secondary Outcomes (27)
Change of questionnaire scores - well-being
30 days (questionnaires will be given to participants several times before, during, and after the intervention.)
Change of questionnaire scores - muscular fatigue
30 days (questionnaires will be given to participants several times before, during, and after the intervention.)
Change of questionnaire scores - vitality
30 days (questionnaires will be given to participants several times before, during, and after the intervention.)
Change of questionnaire scores - rate of fatigue
30 days (questionnaires will be given to participants several times before, during, and after the intervention.)
Change of questionnaire scores - sleep quality
30 days (questionnaires will be given to participants several times before, during, and after the intervention.)
- +22 more secondary outcomes
Study Arms (3)
HIIT-HV
EXPERIMENTALHIIT-HV - high intensity interval training high volume Participants complete a total of 10 HIIT sessions over a 7-day period consisting of 5 x 4-minute intervals at an intensity of 90-95% of their individual maximum heart rate (HRmax), interspersed with a 2.5-minute active recovery period. Each training session is followed by 30 minutes of low-intensity training (total of 300 minutes of additional low-intensity training during this period).
HIIT-LV
EXPERIMENTALHIIT- LV - high intensity interval training low volume Participants complete a total of 10 HIIT sessions over a 7-day period consisting of 5 x 4-minute intervals at an intensity of 90-95% of their individual maximum heart rate (HRmax), interspersed with a 2.5-minute active recovery period.
Control group
NO INTERVENTIONParticipants continue with their regular training program.
Interventions
Eligibility Criteria
You may qualify if:
- Female or male
- aged 18-45 years
- Proof of physical fitness (e.g. sports medical examination required) for measurements with higher intensities (e.g. endurance tests, competition simulation)
- Competition experience at the national or international level in an endurance sport
- VO2max ≥50ml/kg/min for females; ≥55 ml/kg/min for males or a 5-kilometer (km) time trial performance of ≤ 20:00 min (female), or ≤ 18:30 min (male)
You may not qualify if:
- Systemic disease or other known pathology in the organs: heart, lungs, kidney, stomach, spleen, liver, gall bladder, and intestines.
- Evidence of pulmonary disease: forced expiratory volume in one second/forced expiratory volume \< 70% with/without symptoms (cough, sputum) or other evidence of pulmonologic disease.
- Diabetes II.
- Neurological or psychological disease of any kind.
- Currently undergoing medical or psycho-therapeutic treatment.
- Health condition that does not allow regular participation in the training forms (e.g. acute illnesses such as fever or other flu-like infections within the last 7 days before the start of the study), orthopedic diseases, injuries to the muscular, bone, joint or tendon apparatus within the last three months.
- Alcohol or drug abuse.
- Already high training volume with high intensity training (more than 2 weekly training sessions of high-intensity training)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Salzburglead
- Paracelsus Medical Universitycollaborator
- Johannes Gutenberg University Mainzcollaborator
Study Sites (1)
University of Salzburg
Salzburg, 5400, Austria
Related Publications (4)
Tomaskovic A, Strepp T, Stoggl TL, Neuberger EWI, Simon P, Haller N. Acute and Chronic Effects of a High-Intensity Interval Training Shock Microcycle on Cell-Free DNA: A Randomized Controlled Trial. Sports Med Open. 2025 Nov 21;11(1):132. doi: 10.1186/s40798-025-00923-9.
PMID: 41269434DERIVEDStrepp T, Blumkaitis JC, Sareban M, Stoggl TL, Haller N. Training Intensity Distribution of a 7-Day HIIT Shock Microcycle: Is Time in the "Red Zone" Crucial for Maximizing Endurance Performance? A Randomized Controlled Trial. Sports Med Open. 2024 Sep 5;10(1):97. doi: 10.1186/s40798-024-00761-1.
PMID: 39235639DERIVEDStrepp T, Blumkaitis JC, Haller N, Stoggl TL. Adding LIT to HIIT: Is Low-Intensity Training Vital for Endurance-Trained Athletes during a 7-day HIIT Shock Microcycle? Med Sci Sports Exerc. 2024 Aug 1;56(8):1408-1421. doi: 10.1249/MSS.0000000000003435. Epub 2024 Apr 6.
PMID: 38587921DERIVEDStoggl TL, Blumkaitis JC, Strepp T, Sareban M, Simon P, Neuberger EWI, Finkenzeller T, Nunes N, Aglas L, Haller N. The Salzburg 10/7 HIIT shock cycle study: the effects of a 7-day high-intensity interval training shock microcycle with or without additional low-intensity training on endurance performance, well-being, stress and recovery in endurance trained athletes-study protocol of a randomized controlled trial. BMC Sports Sci Med Rehabil. 2022 May 7;14(1):84. doi: 10.1186/s13102-022-00456-8.
PMID: 35526065DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Thomas Stoeggl, Professor, PhD
University of Salzburg
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Researcher
Study Record Dates
First Submitted
September 6, 2021
First Posted
October 5, 2021
Study Start
August 15, 2021
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
January 31, 2024
Record last verified: 2024-01
Data Sharing
- IPD Sharing
- Will not share