Correlation of Anti-gravity Muscle Strength With Glycemic Control, Duration of Disease, and Neuropathy Severity in Type 2 Diabetes Mellitus. (T2DM-AMS)
Correlation of Anti-Gravity Muscle Strength With Glycemic Control, Duration of Disease, and Neuropathy Severity in Type 2 Diabetes Mellitus.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The objective of the present study was to determine the effects of high-intensity interval training on cognitive flexibility among female teenagers. The current study suggests that the high intensity physical training improves the cognitive ability of the participants. Evidence indicates that regular physical activity and high intensity interval training improves the physical strengthening and corresponding improvements in cardiopulmonary physical fitness that results in the increase in cerebral perfusion and vasoreactivity across the human lifespan. The betterment in the cerebral perfusion leads to better cognitive ability and mental health.
The physical activity program comprises 8 weeks consisting of Low-intensity interval training in the first week to high-intensity interval training in the 8th week. Participants of the two groups i.e., experimental and control groups were assessed at baseline fourth and eighth week by Digital Span and Mini mental state examination.
The current study from the statistical analysis suggests that better results are obtained by high intensity physical activity among the female teenagers overtime both in terms of cognitive ability and physical strength.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Sindh
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Sukkur, Sindh, Pakistan, 65200
- RIPRS
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Experimental (High Intensity Interval Training)
High Intensity Interval Training for 8 weeks, which include lunges, squatting sprinting and other exercises.
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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
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Control (No Intervention)
Control Group received no intervention they all will be engaged in normal daily routines.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Digit Span (DGS)
Time Frame: Baseline to 8 weeks
|
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
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Baseline to 8 weeks
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Mini Mental State Examination (MMSE)
Time Frame: Baseline to 8 weeks
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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.
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Baseline to 8 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Waqar Ahmed Awan, PhD, Faculty of Rehabilitation & Allied Health Sciences, Riphah International University
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
- RIPHAH/FR&AHS/Letter-014841
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
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