- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05865145
Effects of Aerobic Exercise on Basic Metabolic Panel Perceived Exertion and Exercise Adherence in Elderly
Effects of Two Different Intensities of Aerobic Exercise on Basic Metabolic Panel Perceived Exertion and Exercise Adherence in Older Obese Adults
Participants were randomly assigned to two groups prior to their second visit:
the High intensity interval training group A (HIIT) and Low intensity interval training group B (LIIT).
The randomization processes were conducted in Excel utilizing a random-number generator. Prior to the second visit, each participants' target exercise heart rate ranges were determined.
Group A will receive a program of high intensity interval training program Group B will receive a program of Low intensity interval training program
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rana H Elbanna, PHD
- Phone Number: 002 01062070686
- Email: rana.hesham@pt.cu.edu.eg
Study Contact Backup
- Name: Sherif O Elabd
- Phone Number: 002 01067227404
- Email: sherif.osama@muc.edu.com
Study Locations
-
-
-
Giza, Egypt, 12613
- Recruiting
- Outpatient clinic faculty of physical therapy at Cairo University
-
Contact:
- Sherif O osama, PHD
- Phone Number: 00201067227404
- Email: shiref.elabd@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- could stand and walk for 30m without becoming out of breath.
- could walk safely without the aid of another person.
- body mass index (BMI) ≥ 30 kg/m2
Exclusion Criteria:
- uncontrolled preexisting health conditions such as:
- uncontrolled hypertension
- uncontrolled diabetes
- uncontrolled heart disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group A
will receive High Intensity Interval Training program
|
Electronic Bicycle equipped with electronic break, display screen, adjustable seat, handle bar and foot straps will be adjusted for High or Low interval intensity training.
|
Experimental: Group B
will receive Low Intensity Interval Training program
|
Electronic Bicycle equipped with electronic break, display screen, adjustable seat, handle bar and foot straps will be adjusted for High or Low interval intensity training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Perceived Exertion
Time Frame: 4 weeks
|
The Modified Borg Dyspnea Scale was used to assess perceived exertion during breathing.
It was given after the first and final training sessions.
The participants were asked to score their difficulty in breathing on a scale of 0 to 10, with 0 indicating no trouble in breathing at all and 10 indicating maximum difficulty in breathing
|
4 weeks
|
Exercise Adherence
Time Frame: 4 weeks
|
The Exercise Adherence Rating Scale (EARS) is a self-reported 16-item questionnaire that rates adherence to prescribed workouts.
The EARS are divided into three components.
The suggested exercise questionnaire is discussed in Section (A), Section (B) discusses exercise adherence behavior, and Section (C) discusses the factors for exercise adherence/non-adherence.
All items in sections B and C are rated on a 5-point Likert scale (0 = fully agree to 4 = entirely disagree).
Section 'B' favourably phrased items (items 1, 4, and 6) and Section 'C' positively phrased items (items 4, 5, 6, and 7) are assessed in reverse order.
Sections "B" and "C" have possible total scores ranging from 0 to 24 and 0 to 40, respectively.
The potential total score for parts (B) and (C) is 64.
A higher total score suggests more adherence to exercise.
|
4 weeks
|
Glucose level
Time Frame: 4 weeks
|
blood test that examines Glucose level in (mmol/L)
|
4 weeks
|
calcium level
Time Frame: 4 weeks
|
blood test that examines calcium level in (mg/dL)
|
4 weeks
|
sodium level
Time Frame: 4 weeks
|
blood test that examines sodium level in (mmol/L)
|
4 weeks
|
potassium level
Time Frame: 4 weeks
|
blood test that examines potassium level in (millimol/L)
|
4 weeks
|
carbon dioxide level
Time Frame: 4 weeks
|
blood test that examines carbon dioxide level in parts per million (ppm)
|
4 weeks
|
chloride level
Time Frame: 4 weeks
|
blood test that examines chloride level in mmol/L
|
4 weeks
|
blood urea nitrogen (BUN) level
Time Frame: 4 weeks
|
blood test that examines blood urea nitrogen (BUN) level in (mg/dL)
|
4 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- DR Rana
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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