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Effect Of Resistive Exercises Versus Aerobic Exercises On Varicose Veins In Postmenopausal Women

Not Applicable
Completed
Conditions
Varicose Veins
Interventions
Other: Life style modification advice
Other: Aerobic exercises
Other: Resistive exercise
Registration Number
NCT06271798
Lead Sponsor
Cairo University
Brief Summary

The purpose of this study will be to determine the effect of resistive exercises on varicose veins in postmenopausal women, the effect of aerobic exercise on varicose veins in postmenopausal women and to compare between the effect of resistive exercise versus aerobic exercise on varicose veins in post menopausal women.

Detailed Description

Varicose veins in the lower extremities present a spectrum of symptoms from cosmetic issues to severe discomfort including telangiectases, reticular veins, edema, pigmentation, and venous ulceration. These veins lead to painful swelling, skin discoloration, and potential complications like thrombosis, and nerve injury, impacting an individual's efficiency and life quality. Exercise, particularly aerobic and resistance training, has shown promise in improving pain severity, functional ability, and venous blood flow.

So, the current study will be conducted to compare between the effect of resistive exercises versus aerobic exercises on varicose veins in postmenopausal women.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
44
Inclusion Criteria

Not provided

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Exclusion Criteria
  • Had history of serious vascular disease as deep venous thrombosis.
  • Sensory deficient
  • Any dermatological condition that interferes with the procedure.
  • Any musculoskeletal or neurological disorders.
  • Acute or healed ulcer wounds.
  • Any heart disease or pulmonary disease.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group A (Resistive exercise group):Life style modification adviceThey will receive life style modification advice, in addition to performing resistive exercise three times per week for six weeks.
Group B (Aerobic exercise group):Aerobic exercisesThey will receive the same life style modification advice, in addition to performing aerobic exercise three times per week for six weeks.
Group A (Resistive exercise group):Resistive exerciseThey will receive life style modification advice, in addition to performing resistive exercise three times per week for six weeks.
Group B (Aerobic exercise group):Life style modification adviceThey will receive the same life style modification advice, in addition to performing aerobic exercise three times per week for six weeks.
Primary Outcome Measures
NameTimeMethod
Peak popliteal vein velocity6 weeks

It will be assessed by Doppler ultrasound scan for each woman in both groups before and after treatment.

Secondary Outcome Measures
NameTimeMethod
Visual analogue scale6 weeks

It will be used to assess the leg pain intensity for each woman in both groups before and after treatment. The visual analogue scale is a 10 cm line with anchor statements on the left (no pain) and on the right (extra pain). Patients will be asked to mark their current pain level on the line.Then, the centimeters will be measured from the left end of the line to the marked point to obtain the score of leg pain intensity.

Chronic Venous Disease Quality of Life Questionnaire (CIVIQ-20)6 weeks

It will be used to assess the quality of life for each woman in both groups before and after treatment. Patients will complete the self- questionnaire CIVIQ-20 in the waiting room. The secretary will hand out the questionnaire and collect it once completed. No particular assistance will be provided to patients. This procedure will be chosen on purpose to avoid any interference from an investigator. At study times, symptom severity will be quantified using a four-point scale (0 = absent, 1 = mild, 2 = significant, 3 = severe) for sensation of swelling, cramps and leg heaviness. The scores of CIVIQ-20 range from 0, the worst score, to 100, the best score.

6-minute. walk test6 weeks

It is a sub-maximal test that will be used to assess the aerobic capacity and daily living activity for each woman in both groups before and after treatment procedures.

Trial Locations

Locations (1)

Cairo University

🇪🇬

Giza, Egypt

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