- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06427616
Moderate Intensity Soleus Pushups Versus Sustained Soleus Pushups on Blood Glucose Level Among Young Population
Effects of Short Duration Moderate Intensity Soleus Pushups Versus Sustained Soleus Pushups on Blood Glucose Level Among Young Population
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The soleus muscle is a slow oxidative muscle which possesses molecular machinery necessary for regulating blood borne substrates. It has the ability to increase the local oxidative metabolism for a long period of time without experiencing fatigue. The uniqueness lies in this muscle because of its inability to store glycogen and derives its energy directly from the glucose present in the bloodstream. This in turn helps in lowering the blood sugar by using the excess blood glucose as its primary source of fuel. The soleus muscle also stands out because of its high composition of slow oxidative fibers, around 88% of the fibers are slow twitch fibers, making it the only muscle in human body containing greater proportion of slow twitch fiber.
A specific exercise called soleus push-ups (SPU) can have a huge impact on boosting metabolism and regulating blood glucose level better than the total body muscle exercises, intermittent fasting, weight loss etc. According to the previous study it showed a significant effect on the overall blood chemistry when performed for 270 mins.
So,the purpose of this study will be to find the comparison of acute effects of sustained soleus push-ups with moderate resisted soleus push-ups on blood sugar level. To find whether moderate resisted soleus push-ups will give same or better results in short period of time.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Waqar Ahmed Awan, PHD
- Phone Number: 0333-534884
- Email: waqar.ahmed@riphah.edu.pk
Study Contact Backup
- Name: Sara Noor, DPT
- Phone Number: 0306-1515493
- Email: saramoghal58@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46120
- Recruiting
- Railway General Hospital
-
Contact:
- Waqar Ahmed Awan, PHD
- Phone Number: 03335348846
- Email: waqar.ahmed@riphah.edu.pk
-
Contact:
- Sara Noor, Masters
- Phone Number: 03061515493
- Email: saramoghal58@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age: 18-35 years.
- Gender: both male and female.
- Healthy young adults.
- BMI: healthy weight.
Exclusion Criteria:
- Patient with cardiac issues.
- Any neurological issues.
- Knee injuries.
- Patient with any lower limb injuries.
- DVT and lower amputation.
- Any known diabetic patient.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Short Duration Moderate Intensity Soleus Push-ups (Group A)
Moderate intensity involving weighted soleus push-ups is performed till patient MHR is achieved.
|
Participants will start soleus push-ups in sitting positions. To do so, the participants will be in a seated position, the legs will be at 90 degrees to the floor, feet will be placed flat on the ground. Participants will then move their heels up and down continuously. Soleus push-ups will be performed with moderate intensity using weights which will be placed on their laps. Participants will perform this activity till their 60-80% of their maximum heart rate is achieved and maintained
Other Names:
|
Experimental: Sustained Soleus Push-ups (Group B)
Sustained soleus push-ups will be performed for up to 270 min.
|
Participants will start soleus push-ups in sitting. To do so, the participants will be in a seated position, the legs will be at 90 degrees to the floor, and feet will be placed flat on the ground. Participants will then move their heels up and down continuously for. Sustained soleus push-ups will be performed with light intensity for up to 270 mins. No external resistance will be added. Participants will be provided with a maximum of 4 min break time after every 90 mins intervention. In the meantime, their blood sample will be collected
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Blood Sugar Level
Time Frame: Baseline to 6 hours
|
The primary outcome measure will be the change in blood sugar level, measured before and after the intervention period.
This will provide insight into the direct impact of short duration moderate intensity soleus push-ups vs sustained soleus push-ups on blood sugar levels among young individuals.
|
Baseline to 6 hours
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adherence to Exercise Protocol
Time Frame: Baseline to 6 hours
|
Adherence to the prescribed exercise will be monitored throughout the intervention period to assess compliance and determine if there are any differences in adherence between the two exercise groups.
|
Baseline to 6 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Waqar Ahmed Awan, PhD, Riphah International University Islamabad
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
- 3547 Sara Noor
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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