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Sedentary BehaviorsNCT07806032

Acute Responses to Walking, Stair Climbing, and Functional Circuit Exercise

A study testing Walking Protocol, Stair Climbing Protocol and Functional Circuit Protocol in people with Sedentary Behaviors, run by Malatya Turgut Ozal University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study evaluated the acute physiological responses to three different exercise modalities in sedentary young men. Participants completed walking, stair climbing, and functional circuit exercise sessions in a randomized crossover design. Read more about this study

Who is it for?
Ages 18 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Sedentary Behaviors
What is being tested?
Walking Protocol, Stair Climbing Protocol and Functional Circuit Protocol
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
22 Jun 2026to 5 Aug 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male sex.
  • Aged 18-30 years.
  • Classified as sedentary/insufficiently active according to the study eligibility criteria.
  • Able to safely complete the exercise protocols and study assessments.
  • Provided voluntary informed consent.

Who cannot join

  • Current cigarette or electronic cigarette use.
  • Known cardiovascular, respiratory, or metabolic disease.
  • Regular medication use that could affect physiological responses to exercise.
  • Acute infection within the previous 2 weeks.
  • Musculoskeletal conditions that could interfere with safe participation in the exercise protocols.
  • Any condition requiring medical evaluation before exercise participation.
  • Inability to obtain acceptable baseline spirometry measurements according to the study procedures.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Malatya Turgut Ozal University

    Malatya, Malatya, 44100

Other trials in Turkey (Türkiye)

About this study

Official title: Acute Metabolic, Respiratory, and Neuromotor Responses to Walking, Stair Climbing, and Functional Circuit Exercise in Sedentary Individuals: A Heart Rate-Controlled Randomized Crossover Study

This study evaluated the acute physiological responses to three different exercise modalities in sedentary young men. Participants completed walking, stair climbing, and functional circuit exercise sessions in a randomized crossover design. Each exercise session lasted 20 minutes and was performed at a target intensity of 50% heart rate reserve (±5 beats/min), with at least 72 hours between sessions.

The study compared acute respiratory, metabolic, and neuromotor responses to the three exercise modalities. Pulmonary function was assessed using spirometry, blood lactate concentration was measured using capillary blood samples, and countermovement jump performance was assessed as an indicator of neuromuscular performance. Heart rate was continuously monitored during each exercise session.

Being tested
Walking Protocol, Stair Climbing Protocol, Functional Circuit Protocol
Keywords
Walking, Stair Climbing, Functional Exercise, Heart Rate Reserve, Pulmonary Function, Blood Lactate, Countermovement Jump, Sedentary Adults
Medical subject headings
Sedentary Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Walking ProtocolBehavioural

    Also called WP

    Participants performed a 20-minute walking exercise session at a target intensity of 50% heart rate reserve (HRR), maintained within ±5 beats/min of the individual target heart rate. Heart rate was continuously monitored throughout the exercise session.

  • Stair Climbing ProtocolBehavioural

    Also called SP

    Participants performed a 20-minute stair climbing exercise session at a target intensity of 50% heart rate reserve (HRR), maintained within ±5 beats/min of the individual target heart rate. Heart rate was continuously monitored throughout the exercise session.

  • Functional Circuit ProtocolBehavioural

    Also called FCP

    Participants performed a 20-minute functional circuit exercise session at a target intensity of 50% heart rate reserve (HRR), maintained within ±5 beats/min of the individual target heart rate. The circuit consisted of chair sit-to-stand, reverse lunges, wall push-ups, high-knee marching, and low-impact mountain climbers performed on an elevated surface. Heart rate was continuously monitored throughout the exercise session.

Study groups in NCT07806032
Study groupRoleWhat they receive
WP-SP-FCP SequenceExperimentalParticipants completed the Walking Protocol first, followed by the Stair Climbing Protocol and then the Functional Circuit Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol
WP-FCP-SP SequenceExperimentalParticipants completed the Walking Protocol first, followed by the Functional Circuit Protocol and then the Stair Climbing Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol
SP-WP-FCP SequenceExperimentalParticipants completed the Stair Climbing Protocol first, followed by the Walking Protocol and then the Functional Circuit Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol
SP-FCP-WP SequenceExperimentalParticipants completed the Stair Climbing Protocol first, followed by the Functional Circuit Protocol and then the Walking Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol
FCP-WP-SP SequenceExperimentalParticipants completed the Functional Circuit Protocol first, followed by the Walking Protocol and then the Stair Climbing Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol
FCP-SP-WP SequenceExperimentalParticipants completed the Functional Circuit Protocol first, followed by the Stair Climbing Protocol and then the Walking Protocol, with at least 72 hours between sessions.
Receives: Behavioral: Walking Protocol; Behavioral: Stair Climbing Protocol; Behavioral: Functional Circuit Protocol

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Forced Expiratory Volume in One Second (FEV1)

    Forced expiratory volume in one second (FEV1) was measured by spirometry before and 5 minutes after each exercise condition. The primary outcome was the change in FEV1 (ΔFEV1), calculated as post-exercise FEV1 minus pre-exercise FEV1 and expressed in liters (L). Measurements were obtained following standardized spirometry procedures.

    Measured: Baseline and 5 minutes after each exercise session

Secondary outcomes (8)
  1. Change in Forced Vital Capacity (FVC)

    Forced vital capacity (FVC) was measured by spirometry before and 5 minutes after each exercise condition. The outcome was the change in FVC (ΔFVC), calculated as post-exercise FVC minus pre-exercise FVC and expressed in liters (L).

    Measured: Baseline and 5 minutes after each exercise session

  2. Change in FEV1/FVC Ratio

    The FEV1/FVC ratio was assessed by spirometry before and 5 minutes after each exercise condition. The outcome was the change in FEV1/FVC ratio (ΔFEV1/FVC), calculated as the post-exercise value minus the pre-exercise value.

    Measured: Baseline and 5 minutes after each exercise session

  3. Change in Peak Expiratory Flow (PEF)

    Peak expiratory flow (PEF) was measured by spirometry before and 5 minutes after each exercise condition. The outcome was the change in PEF (ΔPEF), calculated as the post-exercise PEF minus the pre-exercise PEF and expressed in liters per second (L/s).

    Measured: Baseline and 5 minutes after each exercise session

  4. Change in Blood Lactate Concentration

    Capillary blood lactate concentration was measured before exercise and 3 minutes after each exercise condition. The outcome was the change in blood lactate concentration (ΔLactate), calculated as the post-exercise value minus the pre-exercise value and expressed in millimoles per liter (mmol/L).

    Measured: Baseline and 3 minutes after each exercise session

  5. Change in Countermovement Jump Height (CMJ)

    Countermovement jump (CMJ) height was assessed before and after each exercise condition. The outcome was the change in CMJ height (ΔCMJ), calculated as the post-exercise value minus the pre-exercise value and expressed in centimeters (cm).

    Measured: Baseline and immediately after post-exercise spirometry initiated at 5 minutes after each exercise session

  6. Mean Heart Rate During Exercise

    Heart rate was continuously monitored throughout each exercise condition. Mean heart rate was calculated across the exercise period and expressed in beats per minute (bpm).

    Measured: During each 20-minute exercise session

  7. Maximum Heart Rate During Exercise

    Heart rate was continuously monitored throughout each exercise condition. Maximum heart rate was defined as the highest heart rate recorded during the exercise period and expressed in beats per minute (bpm).

    Measured: During each 20-minute exercise session

  8. Time Spent in the Target Heart Rate Range

    Heart rate was continuously monitored throughout each exercise condition. The outcome was the percentage of exercise time during which heart rate remained within ±5 beats/min of the individualized target heart rate corresponding to 50% heart rate reserve (HRR)

    Measured: During each 20-minute exercise session

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Sep 2026
  2. Study start22 Jun 2026
  3. Primary completion5 Aug 2026
  4. Study completion5 Aug 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Participants completed three exercise conditions (walking, stair climbing, and functional circuit exercise) in a randomized crossover design. The order of the three conditions was determined using six balanced intervention sequences, with at least 72 hours between exercise sessions.
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07806032
Sponsor's protocol ID
2026/205
Status last verified
Sep 2026
First submitted
1 Sep 2026
Last updated
8 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data are not planned to be shared because no data-sharing plan was established as part of the original study protocol.

Questions about this trial

What is this clinical trial studying?

A study testing Walking Protocol, Stair Climbing Protocol and Functional Circuit Protocol in people with Sedentary Behaviors, run by Malatya Turgut Ozal University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Forced Expiratory Volume in One Second (FEV1) (time frame: Baseline and 5 minutes after each exercise session). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Sep 2026.

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