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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04215133
Other study ID # IstanbulUCe
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 3, 2019
Est. completion date May 20, 2021

Study information

Verified date May 2021
Source Istanbul University-Cerrahpasa
Contact GAMZE AYDIN, MSc
Phone +905377600256
Email gmzetsn@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to evaluate the effect of exercise training in addition to compression therapy on quality of life, venous return time, muscle strength, clinical severity, functional capacity in venous insufficiency compared to compression treatment alone. Fourty-two volunteer patients with venous insufficiency will include in the study were randomly divided into three groups as inspiratory exercise, calf muscle exercise and control. While the control group will receive only compression therapy, the inspiratory exercise group will apply inspiratory muscle training consisted of strengthening exercise in addition to compression therapy; kalf muscle exercise group will apply strengthening exercise for calf muscle in addition to compression therapy for 2 days/week with physiotherapist and 3 days/week by themselves, 8 weeks. All the patients will assess with Chronic Venous Disease Quality of life Questionnaire-20 (CIVIQ-20), Nottingham Health Profile, Photopletismograph, Venous Clinical Severity Score (VCSS), hand-held dynamometer, Visual Analogue Scale (VAS), circumference measurements, 6-minute walk test (6MWT), before and after the treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 42
Est. completion date May 20, 2021
Est. primary completion date May 14, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Diagnosis of venous insufficiency between 18-75 years with duplex ultrasound imaging - CEAP classification used in venous insufficiency is C2-C3-C4-C5 - Having written and verbal communication in Turkish Exclusion Criteria: - Acute deep vein thrombosis - The presence of ulceration - Being in class III and IV according to the New York Heart Association classification - Presence of respiratory failure - Undergoing chemotherapy due to the presence of any cancer - Being in the process of treatment for neurological, orthopedic or rheumatologic diseases including lower extremity

Study Design


Related Conditions & MeSH terms


Intervention

Other:
exercise therapy
inspiratory muscle training consists of strengthening exercise with threshold Inspiratory muscle training device and calf muscle training consist of isotonic and isometric strengthening exercise for calf muscle. All groups will receive compression therapy at the same time.

Locations

Country Name City State
Turkey Istanbul University Cerrahpasa Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University-Cerrahpasa

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Chronic Venous Insufficiency Questionnaire-20 (CIVIQ-20) Quality of life 12 months
Primary Photoplethysmograph (PPG) venous return time 12 months
Secondary Hand held dynamometer muscle strength 12 months
Secondary Venous Clinical Severity Score (VCSS) clinical severity 12 months
Secondary 6 minutes walk test functional capacity 12 months
Secondary digital goniometer range of motion of ankle 12 months
Secondary visual analog scale pain 12 months
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