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Changes in oxygenation of skin and muscles after the use of Functional Bandage in women with Varicose Veins

Kinesio Taping use in tissue oxygenation in women with Chronic Venous Insufficiency: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9bhbrp
Enrollment
Unknown
Registered
2018-06-26
Start date
2017-03-14
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Varicose veins of the lower limbs / Chronic venous insufficiency

Interventions

Intervention group: Kinesio taping tapes will be applied with the objective of activating lateral and medial gastrocnemius muscles, using 10 to 15% tension. All applications will be performed by the s
Device
E02.779

Sponsors

Universidade Federal de Minas Gerais
Lead Sponsor
Universidade Federal de Minas Gerais
Collaborator

Eligibility

Sex/Gender
Female
Age
30 Years to 79 Years

Inclusion criteria

Inclusion criteria: Must be female, be between 30 and 79 years old and present the diagnosis of chronic venous insufficiency (confirmed by Duplex Scan) or classified in stages C1, C2 or C3 of CEAP. To be included in the study the participants may not be on hormone replacement therapy and may not have symptoms of intermittent claudication, lymphedema, diagnosis of thrombosis for less than three months, heart failure, and no other type of conservative treatment for IVC, or have undergone sclerotherapy or surgery in the past three months. In addition, they can not present any contraindication to the use of KT such as open sores, trauma, edema arising from heart or kidney disease, cancer, KT allergy, and pregnancy. All participants must agree to participate in the research by signing the Informed Consent Term.

Exclusion criteria

Exclusion criteria: Participants who present knesio taping allergy or intolerance will be excluded.

Design outcomes

Primary

MeasureTime frame
Evaluation of the tissue perfusion variables (oxyhemoglobin, deoxyhemoglobin and peripheral saturation) will be done using the equipment that uses near infrared (NIRS), model Portamon System (Artinis®, The Netherlands). Evaluations will be done at the beginning and after four weeks of treatment. The first evaluation will take place in two days. Measurements of tissue perfusion with NIRS will be done, venous occlusion's maneuver followed by arterial occlusion's maneuver. In addition to the measurement during treadmill tests, plethysmography movement, Incremental Shuttle Walk Test and Heel-rise test, these in random order. On the second day (between 48 hours and a maximum of one week) NIRS measurements will be done before and after KT placement (intervention and control). During 30 minutes the tissue oxygenation variables will be measured by the NIRS at rest, and then the participants will again perform the movements and plethysmography. In the GC volunteers KT will be placed in the same places, without the necessary positions and tensions. KT tapes should be replaced three times in the week prior to the exercise protocol in both groups. At the end of the four weeks (totaling twelve meetings), the reevaluation will be carried out respecting the randomization of the tests.

Secondary

MeasureTime frame
Quality of life through the questionnaire: Medical Outcomes Study -36-Item Short-Form Health Survey (SF-36), this being a multidimensional questionnaire, consisting of 36 items, which aims to assess quality of life. It evaluates the following dimensions: functional capacity (ten items), physical appearance (two items), pain (two items), general health status (five items), vitality (four items), mental health Two items) and emotional (three items). ;Edema: through the circumference of the leg. The tape measure will be used to measure the calf diameter, before and after intervention, to compare them and to contact if there was inferential alteration of the edema in the lower limbs. It will be performed in the legs, using as reference three measurement sites: just below the lower pole of the patella, just above the malleoles and at the midpoint between these two measurements.;Symptoms: assessed by visual analogue scale It is an instrument that allows the simple measurement of the intensity of the pain. It is characterized by the use of a 10 cm line containing, at its ends, phrases like "absence of pain" and "unbearable pain". In the present study, the participants will be asked to mark the intensity of the symptoms in the 10cm trait, by means of the questioning: "Mark in this trait the intensity of the sensation that is feeling of heavy, swollen legs, cramps, heat or burning, itching or Tingling. Knowing that the zero (0) is "absence of symptom" and the 10 "unbearable symptom".

Countries

Brazil

Contacts

Public ContactDanielle Aparecida Pereira

Universidade Federal de Minas Gerais

danielleufmg@gmail.com+55 -031-34094592

Outcome results

None listed

Source: REBEC (via WHO ICTRP)