- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06502626
Effects of Sprint Interval Training on Field Hockey Players.
Effects of Sprint Interval Training on Speed, Change of Direction and Running Performance Among Field Hockey Players.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Field hockey is a team sport played with sticks and balls in which players' movements are spontaneous and dictate the fluctuating nature of competitive match play. A number of training programs are used to improve the performance of the athlete. One of the trainings that is used to enhance the performance of a sports person is "Sprint Interval Training" and it consists of short bursts of maximal or supramaximal exercise interspersed with passive rest or light to moderately intense exertion during rebound periods. Sprint interval training dramatically improves anaerobic and aerobic performance in both trained and untrained athletes. The aim of this study is to find the effect of sprint internal training on speed, change of direction and running performance among field hockey players.
A randomized controlled trial will be conducted at Pakistan Sports Academy, Lahore through non-probability convenience sampling technique on 28 players which will be allocated into both interventional and control group. Pre-training values of the players will be recorded by 20 m sprint test for speed, 505 Change of direction test for change of direction and 3000m time trial for running performance. Both groups will perform regular training. Sprint interval training will be given to Group A and regular training will be performed by Group B. Players will perform the training 3 times a week for 4 weeks and treatment evaluation will be done after 4 weeks. Data will be analyzed using SPSS software version 26. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or non-parametric test will be used.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tehreem Sumbal, MS-Spt
- Phone Number: 03202072007
- Email: sumbalmirza9@gmail.com
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 52254
- Recruiting
- Pakistan Sports Academy
-
Contact:
- Amna Shahid, T-DPT
- Phone Number: 03344512823
- Email: amna.shahid@riphah.edu.pk
-
Sub-Investigator:
- Amna Shahid, T-DPT
-
Principal Investigator:
- Tehreem Sumbal, MS-SPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 18-30 years.
- Both males and females.
- Moderate level of training (Approximately 3 hours per week of activity).
- Playing experience of minimum 2 years.
- Being physically active in a self-reported manner (Approximately 150 minutes of physical activity weekly).
Exclusion Criteria:
- Systemic Conditions (unstable angina, systemic arterial hypertension, chronic obstructive pulmonary disease, diabetes mellitus, neoplasm, renal failure and sequelae of stroke).
- Any musculoskeletal issues that made it difficult to follow protocols or conduct testing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sprint Interval Training
Sprint interval training will be given for 4 weeks.
Each week consisted of three training sessions, separated by at least one resting day.
Participants will complete a 15-minutes warm up before training session.
The Sprint interval training group consisted of 30 s sprints at near maximal effort, with three minutes of rest between each sprint.
The training intensity of Sprint interval training sessions was evaluated subjectively during sessions.
During the first week, the Sprint interval training group performed five sprints per session.
The number of sprints then increased gradually, until a total of 10 sprints per session.
When the number of sprints reached seven, subjects were given six minutes of rest midway through the training session
|
Sprint interval training will be given for 4 weeks.
Each week consisted of three training sessions, separated by at least one resting day.
Participants will complete a 15-minutes warm up before training session.
The Sprint interval training group consisted of 30 s sprints at near maximal effort, with three minutes of rest between each sprint.
The training intensity of Sprint interval training sessions was evaluated subjectively during sessions.
During the first week, the Sprint interval training group performed five sprints per session.
The number of sprints then increased gradually, until a total of 10 sprints per session.
When the number of sprints reached seven, subjects were given six minutes of rest midway through the training session
|
|
Other: Regular Training
Regular training will be done.
|
performed their routine programs
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speed
Time Frame: 10 months
|
It will be assessed by 20m sprint test, values will be taken before and after the application of sprint interval training for the participants of both groups.
|
10 months
|
|
Change of direction
Time Frame: 10 months
|
It will be assessed by 505 Change of direction test, values will be taken before and after the application of sprint interval training for the participants of both groups.
|
10 months
|
|
Running performance
Time Frame: 10 months
|
It will be assessed by 3000m time trial, values will be taken before and after the application of sprint interval training for the participants of both groups.
|
10 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amna Shahid, t-DPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- REC/RCR & AHS/23/0477
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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