- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04932733
Isometric Exercises in Healthy Elderly Individuals
January 9, 2022 updated by: Salameh Aldaja
Effects of a Single Session of Knee Isometric Exercises on Blood Pressure in Healthy Elderly: A Clinical Controlled Trial
A total of 58 participants were selected and divided into two groups equally, namely, elderly, and young groups with the age groups of 60-80 years and 20-30 years, respectively.
The Heart Rate (HR), Respiratory Rate (RR), Blood Pressure (BP), Oxygen Saturation (SaO2), and Mean Arterial Pressure (MAP) for each participant were assessed before and after the treatment session.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The elderly participants in the experimental group and the young participants in the control group underwent a single session of 5-minute quadriceps isometric exercise.
The participant was asked to take rest of 10 minutes before performing the exercise.
After that, the exercise was performed from a long-sitting position.
Study Type
Interventional
Enrollment (Actual)
58
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 Locations
-
-
-
Amman, Jordan, 11622
- Isra University
-
-
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
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- The inclusion criteria were normotensive males and females in the above age groups.
Exclusion Criteria:
- Participants with a chronic history of alcohol, smoking, resting tachycardia (>100 beats per min), hypertension, history of any other cardiovascular disorders, any peripheral vascular disease, those on a regular exercise program, and uncooperative participants.
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Elderly isometric exercise
Quadriceps isometric exercise.
|
The elderly participants in the experimental group underwent a single session of 5-minute quadriceps isometric exercise.
The participant was asked to take a rest of 10 minutes before performing the exercise.
After that, the exercise was performed from a long-sitting position.
Other Names:
|
|
Active Comparator: Young isometric exercise
Quadriceps isometric exercise.
|
The young participants in the experimental group underwent a single session of 5-minute quadriceps isometric exercise.
The participant was asked to take a rest of 10 minutes before performing the exercise.
After that, the exercise was performed from a long-sitting position.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood Pressure (BP)
Time Frame: Change from baseline blood pressure at 1 day
|
Both systolic and diastolic blood pressures were measured by a trained physiotherapist in the right upper arm using an appropriate-sized cuff at the baseline and the end of the intervention using an automated Dinamap MPS Select device (Johnson & Johnson, New Brunswick, NJ).
|
Change from baseline blood pressure at 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Respiratory Rate (RR)
Time Frame: Change from baseline respiratory rate at 1 day
|
Respiratory rate was assessed by visually observe for 30 seconds and multiply observed breaths by 2 to obtain breaths per minute (BPM).
|
Change from baseline respiratory rate at 1 day
|
|
Oxygen Saturation (SaO2)
Time Frame: Change from baseline oxygen saturation at 1 day
|
Oxygen saturation was recorded using a finger pulse oximeter.
The sensor was placed on the right index finger, and the values were recorded after at least two minutes.
|
Change from baseline oxygen saturation at 1 day
|
|
Heart Rate (HR)
Time Frame: Change from baseline heart rate at 1 day
|
Heart rate was recorded using a finger pulse oximeter.
The sensor was placed on the right index finger, and the values were recorded after at least two minutes.
|
Change from baseline heart rate at 1 day
|
|
Mean Arterial Pressure (MAP)
Time Frame: Change from baseline mean arterial pressure at 1 day
|
Mean arterial pressure was calculated MAP as diastolic blood pressure (DBP) + 1/3 [systolic blood pressure (SBP) - DBP].
|
Change from baseline mean arterial pressure at 1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Salameh Aldaja, PhD, Isra University
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 (Actual)
February 15, 2021
Primary Completion (Actual)
December 1, 2021
Study Completion (Actual)
December 1, 2021
Study Registration Dates
First Submitted
June 6, 2021
First Submitted That Met QC Criteria
June 12, 2021
First Posted (Actual)
June 21, 2021
Study Record Updates
Last Update Posted (Actual)
January 25, 2022
Last Update Submitted That Met QC Criteria
January 9, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 337-1/1
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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