Effects of Aerobic Exercise on Basic Metabolic Panel Perceived Exertion and Exercise Adherence in Elderly

May 17, 2023 updated by: Rana Elbanna

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

Recruiting

Conditions

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Giza, Egypt, 12613
        • Recruiting
        • Outpatient clinic faculty of physical therapy at Cairo University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

May 1, 2023

Primary Completion (Anticipated)

May 1, 2023

Study Completion (Anticipated)

May 1, 2023

Study Registration Dates

First Submitted

April 5, 2023

First Submitted That Met QC Criteria

May 17, 2023

First Posted (Actual)

May 18, 2023

Study Record Updates

Last Update Posted (Actual)

May 18, 2023

Last Update Submitted That Met QC Criteria

May 17, 2023

Last Verified

May 1, 2023

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

No

Studies a U.S. FDA-regulated device product

No

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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