- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07588893
Buerger-Allen Exercises and Peripheral Circulation in Sedentary Office Workers (BAE-CIRC)
Acute Effects of Buerger-Allen Exercises on Lower Extremity Circulatory Parameters in Sedentary Office Workers: A Single-Group Pretest-Posttest Clinical Trial
Study Overview
Status
Intervention / Treatment
Detailed Description
Sedentary behavior and prolonged sitting are associated with impaired venous return, reduced peripheral blood flow, endothelial dysfunction, and increased cardiovascular risk. Office workers who remain seated for extended periods may experience lower extremity discomfort, edema, and early circulatory impairment.
Buerger-Allen exercises are position-based therapeutic exercises that involve sequential elevation, dependency, and horizontal rest of the lower limbs. These exercises are designed to promote arterial inflow, facilitate venous return, and enhance tissue perfusion without requiring specialized equipment. Previous studies have demonstrated beneficial effects in patients with peripheral vascular disease and diabetes, but evidence regarding their acute effects in healthy sedentary adults is limited.
This study will use a quasi-experimental single-group pretest-posttest design to investigate the immediate effects of Buerger-Allen exercises on lower extremity circulation in sedentary office workers. A total of 35 participants aged 18 to 45 years will be recruited from Istanbul Gelisim University. All participants will complete a standardized 20-minute Buerger-Allen exercise protocol.
Primary outcome measures will include skin surface temperature assessed with infrared thermometry, capillary refill time, ankle-brachial index, peripheral oxygen saturation, and heart rate. Measurements will be performed at baseline, immediately after the intervention, and 10 minutes after the intervention.
The study is expected to provide evidence regarding the effectiveness of a simple and low-cost physiotherapy intervention for improving peripheral circulation and preventing the adverse vascular effects associated with prolonged sedentary behavior.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Busenur KARAGÖZ, MSc
- Phone Number: +90 534 062 71 24
- Email: buse.nur97e@gmail.com
Study Contact Backup
- Name: Gökay ÇAKIROĞLU, PT
- Phone Number: +90 542 519 42 55
- Email: gcakiroglu@gelisim.edu.tr
Study Locations
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-
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Istanbul, Turkey (Türkiye)
- Istanbul Gelisim University
-
Contact:
- Busenur KARAGÖZ, MSc
- Phone Number: +90 534 062 71 24
- Email: buse.nur97e@gmail.com
-
Contact:
- Gökay ÇAKIROĞLU, PT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy sedentary office workers
- Age between 18 and 45 years
- Sitting for at least 6 hours per day for work-related activities
- Not meeting regular physical activity recommendations
- Willing to participate voluntarily and provide written informed consent
Exclusion Criteria:
- History of peripheral arterial disease, deep vein thrombosis, or other vascular disorders
- Cardiovascular, neurological, or musculoskeletal conditions that may affect lower extremity circulation or prevent exercise participation
- Diabetes mellitus
- Current smoking
- Pregnancy
- Use of medications that may significantly affect peripheral circulation
- Lower extremity injury or surgery within the previous 6 months
- Participation in regular structured exercise programs
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Buerger-Allen Exercise Group
Participants will perform a single standardized 20-minute Buerger-Allen exercise session.
Lower extremity circulatory parameters will be assessed before the intervention, immediately after the intervention, and 10 minutes after the intervention.
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The intervention consists of a standardized Buerger-Allen exercise protocol involving three sequential positions: (1) elevation of the lower limbs above heart level to facilitate venous return, (2) dependency of the lower limbs to promote arterial blood flow, and (3) horizontal supine rest to stabilize circulation.
The complete exercise session lasts approximately 20 minutes and is performed once.
Lower extremity circulatory parameters are assessed at baseline, immediately after the intervention, and 10 minutes after the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skin Surface Temperature
Time Frame: Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Skin surface temperature measured with an infrared thermometer in degrees Celsius (°C).
Higher values indicate increased peripheral blood flow and tissue perfusion.
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Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
|
Capillary Refill Time
Time Frame: Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Capillary refill time measured in seconds.
Shorter times indicate improved peripheral microcirculation and tissue perfusion.
|
Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ankle-Brachial Index (ABI)
Time Frame: Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Ratio of ankle to brachial systolic blood pressure used to assess lower extremity arterial circulation.
Higher values within the normal range indicate better arterial perfusion.
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Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
|
Peripheral Oxygen Saturation (SpO₂)
Time Frame: Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Oxygen saturation measured by pulse oximetry and expressed as a percentage (%).
Higher values indicate improved peripheral oxygenation.
|
Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
|
Heart Rate
Time Frame: Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Heart rate measured by pulse oximetry and expressed in beats per minute (bpm).
|
Baseline, Immediately After Intervention, and 10 Minutes After Intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Busenur KARAGÖZ, MSc, Istanbul Gelisim University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IGU-FTR-BAE-2026-001
- 2209A-2025Fall-Submitted (Other Identifier: The Scientific and Technological Research Council of Türkiye (TUBITAK))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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