Effects of High Intensity Interval Training on Cognitive Flexibility Among Female Teenagers
Effects Of High Intensity Interval Training on Cognitve Flexibility Among Female Teenagers
1 other identifier
interventional
40
1 country
1
Brief Summary
The study suggests that the high intensity exercise training program is beneficial for the female teenagers to enhance their cognitive abilities along with the physical strengthening. It also helps the teenagers to increase their mental health for better health and memory.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2023
Shorter than P25 for not_applicable
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
February 6, 2023
CompletedFirst Submitted
Initial submission to the registry
February 9, 2023
CompletedFirst Posted
Study publicly available on registry
May 24, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2023
CompletedAugust 25, 2023
August 1, 2023
6 months
February 9, 2023
August 24, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Digit Span (DGS)
Cognitive Flexibilty was assessed by Digit Span (DGS), is a measure of verbal short-term and working memory that can be used in two formats, Forward Digit Span and Reverse Digit Span. This is a verbal task, with stimuli presented auditory, and responses spoken by the participant and scored accordingly
Baseline to 8 weeks
Mini Mental State Examination (MMSE)
The MMSE is a brief screening tool that provides a quantitative assessment of cognitive impairment and records cognitive changes over time (23). The maximum score for the MMSE is 30. A score of 25 or higher is classed as normal. If the score is below 24, the result is usually considered to be abnormal, indicating possible cognitive impairment.
Baseline to 8 weeks
Study Arms (2)
Experimental (High Intensity Interval Training)
EXPERIMENTALHigh Intensity Interval Training for 8 weeks, which include lunges, squatting sprinting and other exercises.
Control (No Intervention)
NO INTERVENTIONControl Group received no intervention they all will be engaged in normal daily routines.
Interventions
The HIIT sessions ranging from 4-12 minutes in duration for 8 weeks in which three sessions will be conducted each week (weeks 1-3: 4 minutes; weeks 4-6: 8 minutes; weeks 7-8: 12 minutes respectively), with a work to rest ratio of 30sec: 10sec, as mention in table 1. Experimental group/HIT group engaged in their HIIT sessions (inclusive of a short warm-up activity including dynamic exercises i.e., walking/running, 8-10 minutes of HIIT and cool down which include static exercises i.e., shoulder and hip muscle stretches). Session duration and intensity are increased with weekly progression in intervention groups. The high resistance training sessions was be delivered by the researcher to HIT group
Eligibility Criteria
You may qualify if:
- Participants falling in this category would be recruited into the study.
- Female gender only
- Age 13-19 years of female teenagers
- Absence of serious medical or mental illness
- volunteered to participate in this study
You may not qualify if:
- Participants failing to fall in this category would be excluded from the study. Diagnosed Psychiatric illness Acute or Chronic Pain and Infections Known case of bone fragility Unstable cardiovascular disease Severe cognitive, visual, or auditory impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
RIPRS
Sukkur, Sindh, 65200, Pakistan
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Waqar Ahmed Awan, PhD
Faculty of Rehabilitation & Allied Health Sciences, Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- one group is taking intervention and other is control group
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 9, 2023
First Posted
May 24, 2023
Study Start
February 6, 2023
Primary Completion
July 30, 2023
Study Completion
August 15, 2023
Last Updated
August 25, 2023
Record last verified: 2023-08
Data Sharing
- IPD Sharing
- Will not share