Exercise Training in Venous Insufficiency
- Conditions
- Venous Insufficiency
- Interventions
- Other: Exercise TrainingOther: Compression Therapy
- Registration Number
- NCT03755180
- Lead Sponsor
- Istanbul University - Cerrahpasa (IUC)
- Brief Summary
The aim of this study is to evaluate the effects of exercise training in addition to compression therapy on clinical severity, vein diameter, reflux and quality of life in venous insufficiency patients.
- Detailed Description
Volunteers who have been diagnosed with venous insufficiency according to the criteria of inclusion, who applied to Istanbul University Istanbul Medical Faculty Cardiovascular Surgery Department will be included this study.
Participants will be randomly allocated 2 groups using the 'Research Randomizer' website. In both groups, a common evaluation protocol will be applied to the patients.
Exercise training in addition to compression bandages will be applied to first group, compression bandages will be applied to second group.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
- Diagnosis of venous insufficiency with duplex ultrasonography
- Classification of CEAP (Clinical-Etiological-Anatomical-Pathological) used in venous insufficiency is C3-C4-C5-C6
- Ankle-brachial index (ABI) is less than 0.7
- Possibility to communicate in written and verbal in Turkish
- Have a level of cognitive ability to understand the instructions given
- Presence of deep vein thrombosis
- Ulceration or open burn wound in lower extremity greater than 4 cm
- Presence of infected ulceration
- Cardiorespiratory insufficiency
- Orthopedic, rheumatologic or neurological comorbidities restrain the exercise in lower extremity
- Presence of a psychiatric illness requiring the use of prescribed medicines
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group 1 Compression Therapy Exercise Group Group 1 Exercise Training Exercise Group Group 2 Compression Therapy Compression Group
- Primary Outcome Measures
Name Time Method Chronic Venous Disease Quality of Life Questionnaire (CIVIQ) 20 Change from Baseline Quality of Life at 6 weeks. CIVIQ 20 is a disease-related quality of life assessment form especially for chronic venous insufficiency patients. The total score is at least 0 and at most 100, and the higher scores indicate better quality of life.
- Secondary Outcome Measures
Name Time Method Venous Clinical Severity Score (VCSS) Assessment is performed at baseline and six weeks rehabilitation program. The VCSS was subsequently developed as an evaluative instrument that would be responsive to changes in disease severity over time and in response to treatment.The total score is at least 0 and at most 30, and the low scores are positively correlated with the severe clinical condition.
The 6 Minute Walk Test Assessment is performed at baseline and six weeks rehabilitation program. The 6-min walk test (6 MWT) is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.
Duplex Ultrasonography Duplex Ultrasonography results is evaluated at baseline and six weeks rehabilitation program. Duplex Ultrasonography is a form of ultrasound that produces images that differentiate between the body's soft tissues and its fluid-filled structures. Duplex Ultrasonography provides information on vascular diameter and reflux in chronic venous insufficiency patients.
Measurement of Calf Girth Assessment is performed at baseline and six weeks rehabilitation program. Circumference measurements will be recorded at 10 cm intervals of both lower legs.
10-Meter Walk Test Assessment is performed at baseline and six weeks rehabilitation program. The 10mWT is used to assess walking speed in meters/second (m/s) over a short distance.
Assessment of Muscle Strength with Handheld Dynamometer Assessment is performed at baseline and six weeks rehabilitation program. The muscle strength of the gastrocnemius and tibialis anterior muscles will be evaluated using the handheld dynamometer.
Visual Analogue Scale (VAS) Assessment is performed at baseline and six weeks rehabilitation program. The levels of pain felt rest/activity/night will be measured using visual analogue scale (VAS). Patients will be asked to evaluate their pain status with a 10-point scale and high scores are positively correlated with pain.
Short Form 36 (SF-36) Assessment is performed before treatment and after six weeks rehabilitation program. SF-36 is used to assess physical and mental health-related quality of life. The total score is at least 0 and at most 100, and the high scores are positively correlated with the high quality of life.
Trial Locations
- Locations (1)
Istanbul Faculty of Medicine
🇹🇷Istanbul, Fatih, Turkey