Acute Effects of Three Different Types Single Leg Exercise in Copd (COPD)

November 26, 2025 updated by: Elif Kocaaga, Hacettepe University
COPD presents not only respiratory symtoms but also vascular or muscle dysfunction. Exercise training is important for aerobic performance increasing. Generally results show exercise training with both lower limb. Increaed arterial stiffness and muscle oxygenation are observed in COPD. One leg exercise result is not enough to highlight these parameters.

Study Overview

Status

Completed

Conditions

Detailed Description

Acute Effects of Three Different Types Single Leg Exercise in Copd

single bout high intensity interval training

single bout continuous exercise training single bout resistance training

Study Type

Interventional

Enrollment (Actual)

26

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

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
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • COPD patients that applied to physiotherapy
  • cooperate to test
  • no severe ortopedical and neurological disease no severe cardiovascular disease volunteer to study

Exclusion Criteria:

  • have an acute exacerbation
  • hypoxemia [PaO2] <55 mmHg
  • no cooperated to test no volunteer to study having ortophedical and neurological diesase that affecting of tests having severe cardiovascular 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: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: single session one leg exercise intervantion in COPD

first session: single session leg Continuous exercise intervantion will be applied to COPD. Unilaterally single leg continuous exercise will be performed as only one session

second session : single session leg high intensity interval exercise intervantion will be applied to COPD. Unilaterally single leg hııt exercise will be performed as only one session

third sessionsingle session leg resistance exercise intervantion will be applied to COPD. Respirocally leg strength (knee extantion ) exercise will be performed

cycle exercise includes single leg

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
six minute walk test
Time Frame: beginning, day 1
six minute walk test in meter
beginning, day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
cardiopulmonary exercise test
Time Frame: beginning, day 2
VO2 max will be recorded as ml/kg/min will be recorded from incremental cycle cpet test
beginning, day 2
single leg extremity test
Time Frame: beginning, day 3
VO2 max will be recorded as ml/kg/min will be recorded from incremental cycle cpet test
beginning, day 3
lung function
Time Frame: beginning, day 1
FVC in % , FEV1 in %, FEV1/FVC ratio, PEF in % and FEF 25-75 in %
beginning, day 1
muscle strength (isometric)
Time Frame: beginning day 1
quadriceps isometric muscle strength will be recorded as kilogram
beginning day 1
muscle strength (10 repeated max)
Time Frame: beginning, day 1
quadriceps 10 repeated max muscle strength will be recorded as kilogram
beginning, day 1
continous exercise acute (single leg)
Time Frame: beginning day 4
VO2 max will be recorded as ml/kg/min will be performed from incremental cycle exercise at single session
beginning day 4
high intensity interval training acute exercise (single leg)
Time Frame: beginning day 5
VO2 max will be recorded as ml/kg/min will be performed from incremental cycle exercise at single session
beginning day 5
strength training acute exercise (single leg)
Time Frame: beginning day 4,5,6
VO2 max will be recorded as ml/kg/min will be performed from incremental cycle exercise at single session
beginning day 4,5,6
muscle oxygenation
Time Frame: beginning day 4,5,6
minumum muscle oxygenation level will be presented as percentage
beginning day 4,5,6
arterial stifness
Time Frame: beginning day 2,3, 4,5,6
Aıx@75 in %
beginning day 2,3, 4,5,6

Collaborators and Investigators

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

Investigators

  • Principal Investigator: elif kocaaga, ms, Hacettepe University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

March 28, 2025

Study Completion (Actual)

March 28, 2025

Study Registration Dates

First Submitted

May 17, 2024

First Submitted That Met QC Criteria

June 17, 2024

First Posted (Actual)

June 20, 2024

Study Record Updates

Last Update Posted (Estimated)

December 4, 2025

Last Update Submitted That Met QC Criteria

November 26, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • GO23-193

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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