- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07585617
Step-Up vs. Running Exercise at Matched Heart Rate Zones in Sedentary Males
May 12, 2026 updated by: Dicle Aras, Ankara University
Assessment of Cardiovascular, Autonomic, and Isometric Leg Strength Adaptations Following Step-Up Versus Running Exercise at Matched Heart Rate Zones in Sedentary Males
This study compares the effects of two aerobic exercise methods - loaded step-up exercise and treadmill running - on cardiovascular fitness, leg strength, heart rate variability, and recovery in sedentary adult males.
Both exercise groups will train at 80-85% of maximum heart rate, three sessions per week for six weeks.
A control group will not participate in any training.
Measurements of estimated VO₂max, isometric leg strength, resting heart rate, heart rate variability indices, and heart rate recovery will be taken before and after the intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
36
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
-
-
Golbasi
-
Ankara, Golbasi, Turkey (Türkiye)
- Ankara University Faculty of Sport Sciences
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male, aged 18-40 years
- Sedentary - no participation in structured exercise programs for at least 6 months prior to the study
- Free from chronic diseases
- No musculoskeletal injuries or surgical interventions within the last 6 months
Exclusion Criteria:
- Female sex
- Age below 18 or above 40 years
- Participation in structured exercise within the last 6 months
- Presence of chronic disease
- Musculoskeletal injury or surgical intervention within the last 6 months
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Step-up Exercise Group (STP)
Participants performed loaded step-up exercises at 80-85% of maximum heart rate using a load of 20% body weight, 3 sessions per week for 6 weeks with progressive volume.
|
Step-up exercise performed on an adjustable platform at individually assigned heights (35 cm or 40 cm, based on participant height), with a load equal to 20% of body weight, at 80-85% of maximum heart rate, 3 sessions per week for 6 weeks with progressive volume increase.
|
|
Active Comparator: Treadmill Running Group (R)
Participants performed continuous treadmill running at 80-85% of maximum heart rate, 3 sessions per week for 6 weeks with progressive volume.
|
Continuous treadmill running at 80-85% of maximum heart rate, 3 sessions per week for 6 weeks with progressive volume increase.
|
|
No Intervention: Control Group (C)
Participants did not engage in any structured exercise training during the 6-week period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Estimated VO2max
Time Frame: Baseline and 6 weeks
|
Estimated maximal oxygen uptake assessed via Yo-Yo Intermittent Recovery Test Level 1
|
Baseline and 6 weeks
|
|
Isometric Leg Strength
Time Frame: Baseline and 6 weeks
|
Maximum isometric leg strength measured using a Takei back-leg lift dynamometer
|
Baseline and 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart Rate Variability
Time Frame: Baseline and 6 weeks
|
HRV indices including pNN50 and MeanRR measured via Polar H10 during supine rest
|
Baseline and 6 weeks
|
|
Heart Rate Recovery
Time Frame: Weeks 1 through 6
|
Time to recovery after and between sets of exercise sessions measured weekly across the 6-week intervention
|
Weeks 1 through 6
|
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 (Actual)
February 20, 2024
Primary Completion (Actual)
May 28, 2024
Study Completion (Actual)
June 10, 2024
Study Registration Dates
First Submitted
May 6, 2026
First Submitted That Met QC Criteria
May 12, 2026
First Posted (Actual)
May 14, 2026
Study Record Updates
Last Update Posted (Actual)
May 14, 2026
Last Update Submitted That Met QC Criteria
May 12, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AUFS-2024-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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