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Efficacy of Active Versus Passive Methods in Chronic Venous Insufficiency

Comparison of the Efficacy of Active Versus Passive Methods in Patients With Chronic Venous Insufficiency

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05383469
Enrollment
66
Registered
2022-05-20
Start date
2022-09-13
Completion date
2023-09-02
Last updated
2023-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Venous Insufficiency

Keywords

exercise, compression, neuromuscular electrical stimulation, massage

Brief summary

The aim of our study was to compare the effectiveness of active and passive practices in patients with CVI.

Detailed description

Volunteers who have been diagnosed with venous insufficiency according to the criteria of inclusion, who applied to Cardiovascular Surgery Department will be included this study. Participants will be randomly allocated 3 groups using the 'Research Randomizer' website. In all groups, a common evaluation protocol will be applied to the patients. Compression therapy will be applied to the first group. Active treatment in addition to compression therapy will be applied to the second group. Passive treatment in addition to compression therapy will be applied to the third group.

Interventions

OTHERExercise Training

Endurance training with a resistance-free bicycle ergometer Strength training with bodyweight Non-resistance ankle pumping exercises

OTHERMassage

Classical massage including superficial and deep stroking and friction methods for the lower extremity.

OTHERNeuromuscular Electrical Stimulation

Symmetrical biphasic current at a frequency of 30-85 Hz

Compression therapy is a treatment applied to patients in the form of Four Layer Compression Bandage and Compression Stocking. Four Layer Compression Bandage is a treatment that requires four different types of bandages. The compression stocking is an elastic stock with various tension and length.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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 the lower extremity * Presence of a psychiatric illness requiring the use of prescribed medicines

Design outcomes

Primary

MeasureTime frameDescription
Circumference measurementsChange from Baseline circumferences at 8 weeks.Circumference measurements will be recorded at 4 cm intervals to evaluated to edema.

Secondary

MeasureTime frameDescription
Venous Clinical Severity Score (VCSS)Assessment will be performed tat baseline and at 8 weeks.Clinical severity will be measured by Venous Clinical Severity Score (VCSS).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.
Handheld DynamometerAssessment will be performed at baseline and at 8 weeks.The muscle strength of the gastrocnemius and tibialis anterior muscles will be evaluated using the handheld dynamometer.
Visual Analogue Scale (VAS)Assessment will be performed at baseline and at 8 weeks.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.
10-Meter Walking TestAssessment will be performed at baseline and at 8 weeks.Walking speed will be evaluated with the 10-meter walking test. 10-meter walking test is used to assess walking speed in meters/second (m/s) over a short distance.
Chronic Venous Disease Quality of Life Questionnaire (CIVIQ) 20Assessment will be performed at baseline and at 8 weeks.Quality of Life will be evaluated with the Chronic Venous Disease Quality of Life Questionnaire (CIVIQ) 20. 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.
6-Minute Walking TestAssessment will be performed at baseline and at 8 weeks.Functional capacity will be evaluated with the 6-minute walking test. The 6-minute walking test (6 MWT) is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026