- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07433348
Effects of High-Intensity Interval Training on Physical and Physiological Parameters in Adolescent Female Field Hockey Players (HIIT IN HOCKEY)
The Effect of the Intensive Interval Training Method Applied to Hockey Players on Certain Physical and Physiological Parameters
Effects of High-Intensity Interval Training on Physical and Physiological Parameters in Adolescent Female Field Hockey Players
High-Intensity Interval Training (HIIT) is a training method that alternates short periods of intense exercise with recovery periods. It is commonly used to improve athletic performance.
This study investigated the effects of an 8-week HIIT program on physical and physiological performance in adolescent female field hockey players. Participants were divided into two groups: one group continued their regular field hockey training, while the other group completed additional HIIT sessions three times per week.
After the intervention, the HIIT group demonstrated improvements in aerobic capacity (VO₂max), reaction time, balance, and standing long jump performance. A decrease in flexibility was observed in this group. The control group showed reductions in aerobic capacity and flexibility.
The findings suggest that adding HIIT to regular field hockey training may improve several key performance parameters in adolescent female athletes.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Adana, Turkey (Türkiye)
- Adana Çukurova Athletics Stadium
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Who have been playing field hockey for at least two years
- Who participated in at least 85% of the training sessions were included in the study.
Exclusion Criteria:
- Those with musculoskeletal injuries or undergoing physical rehabilitation therapy that interfered with their normal physical performance
- Those with permanent or temporary contraindications to physical activity
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
High-Intensity Interval Training (HIIT)
|
Circumstances distinguishing this study from other studies: Although there are studies in the literature stating that HIIT programs improve physical and physiological performance parameters in many branch athletes, there are limited studies specific to the hockey branch. The HIIT programs used in the study are simple and easy in terms of application. |
|
No Intervention: control group
The control group continued with regular hockey training sessions for 8 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximum Oxygen Consumption (VO₂max)
Time Frame: Baseline and Week 8
|
Maximum oxygen consumption measured to evaluate aerobic capacity of the participants.
|
Baseline and Week 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Static Balance
Time Frame: Baseline and Week 8
|
Static balance performance measured using a standardized balance test.
|
Baseline and Week 8
|
|
Reaction time
Time Frame: Baseline and Week 8
|
Reaction time measured using a standardized reaction test to assess neuromuscular performance.
|
Baseline and Week 8
|
|
Flexibility
Time Frame: Baseline and Week 8
|
Flexibility assessed using a standardized sit-and-reach test.
|
Baseline and Week 8
|
|
Standing Long Jump
Time Frame: Baseline and Week 8
|
Standing long jump distance measured to evaluate lower-body explosive power.
|
Baseline and Week 8
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 05/12/2023-2023/12-27
- 2023/12-27 (Other Identifier: Mardin Artuklu University Non-Interventional Clinical Research Ethics Committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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