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Use of the Unstable Shoes in Lower Limb Lymphedema.

Primary Purpose

Lower Limb Lymphedema

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
To compare the efficacy of unstable shoes with that of conventional sports shoes in people with lower-limb primary and secondary lymphedema.
Sponsored by
Universidad Europea de Madrid
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Lower Limb Lymphedema

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: -Subjects affected with lower limb lymphedema -primary, secondary, unilateral or bilateral-, -Daily use of a compression stocking Exclusion Criteria: Subjects with acute infection of the affected limb that did not had any treatment for lymphedema one year prior to the study, Weight <40kg, shoe size <EU35 or >EU47 that have previously used unstable shoes vestibular alterations, vertigo, hypoacusis visual compromise that affects balanc

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Unstable shoes

    Usual sports footwear

    Arm Description

    Use of unstable shoes for 8 weeks

    Use of conventional shoes for 8 weeks

    Outcomes

    Primary Outcome Measures

    Volume of the lower limb
    Volume of the lower limb

    Secondary Outcome Measures

    Circumference measure of the foot
    Circumference measure of the foot
    Changes in lymphedema symptoms
    Changes in lymphedema symptoms

    Full Information

    First Posted
    July 28, 2023
    Last Updated
    August 10, 2023
    Sponsor
    Universidad Europea de Madrid
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05996939
    Brief Title
    Use of the Unstable Shoes in Lower Limb Lymphedema.
    Official Title
    Effectiveness of Unstable Shoes on Volume and Quality of Life in Lower Limb Lymphedema.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    November 1, 2013 (Actual)
    Primary Completion Date
    June 30, 2016 (Actual)
    Study Completion Date
    June 30, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Universidad Europea de Madrid

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Lymphedema is an external manifestation of lymphatic system insufficiency and deranged lymph transport. It is defined as accumulation in the extracellular space of protein-rich fluid, due to a mechanical failure of the lymphatic system. Lymphedema directly affects the quality of life of the patient, not only in the physical aspect, but also in the psychological, sexual and social aspects. Muscle and joint pumps are important external mechanisms of lymphatic and venous fluid return improvement. The unstable shoes demands, especially during standing, increased muscle activity in the lower extremities. A clinical trial was carried out comparing both kinds of footwear, the objective being to evaluate possible differences in the evolution of lymphedema. Unstable shoes (MBT®) were compared with conventional sports shoes. During a clinical trial lasting eight weeks, we assessed quality of life, limb volume, and symptoms derived from lymphedema. The results suggested that the use of unstable shoes is recommendable for walking and for long periods of standing, since it decreases leg cramping and paraesthesia of affected limbs.
    Detailed Description
    Participants Subjects were recruited amongst the members of a Spanish association of people affected with lymphedema. Inclusion criteria were a) Subjects affected with lower limb lymphedema -primary, secondary, unilateral or bilateral-, b) Daily use of a compression stocking. Exclusion criteria were a) Subjects with acute infection of the affected limb b) that did not had any treatment for lymphedema one year prior to the study, c) Weight <40kg, d) shoe size <EU35 or >EU47 e)that have previously used unstable shoes f) vestibular alterations, vertigo, hypoacusis c) visual compromise that affects balance. Procedure Written informed consent was obtained from the participants before the intervention. Random allocation to experimental and control group, was performed using Excel built-in function RAND ().. The generated sequence was employed to allocate the participants to one of the trial groups (e.g., intervention or control). Participants followed an 8 week intervention. Experimental group (EG) were provided with unstable sole shoes (MBT®, Masai Barefoot Technology Spain SL,08021 Spain.) and asked to wear them following a standardized protocol: 1 hour on day 1, increasing 1h each 2 days until 4h of daily use are achieved, during standing position and walking in the context of daily live activities, excluding sport activities. Control group (CG) was provided with a conventional sole sports footwear, following the same protocol that EG. Outcome measures Circumferencial measure. Circumferencial measure was evaluated using a tape measure to measure the circumference of the foot at different points. Distal (4 cm from the base of the nail towards proximal) and Proximal (4 cm from the previous measurement). Volume. Kuhnke's formula was used to calculate the estimated volume of the affected limb(241) V=(C12 + C22 +… Cn2)/π, Where V represents the volume and C refers to the different diameters of the limb, measured in centimeters. Perception of the participants' clinical manifestations (243): measured through a questionnaire on perception of the state of the person's vascular alteration referred to the affected limb. In this survey, the subject is asked to value their symptoms (included heaviness, spider veins, swelling, pain, appearance of varicose veins, cramps, paresthesia and venous ulcers) with a 4-point scale: 0=absent, 1=mild/moderate, 2=important, 3=severe. In addition to lower limb swelling, other important symptoms experienced are heaviness, tightness, and pain. As there is no validated scale or survey to measure these symptoms characteristic of lymphedema, we used as a reference a previous study [10], where the symptoms or clinical manifestations compatible with chronic venous insufficiency that can be extrapolated to lymphedema are described. In addition, a Change of habits survey was conducted at the end of the intervention period

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Lower Limb Lymphedema

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    26 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Unstable shoes
    Arm Type
    Experimental
    Arm Description
    Use of unstable shoes for 8 weeks
    Arm Title
    Usual sports footwear
    Arm Type
    No Intervention
    Arm Description
    Use of conventional shoes for 8 weeks
    Intervention Type
    Other
    Intervention Name(s)
    To compare the efficacy of unstable shoes with that of conventional sports shoes in people with lower-limb primary and secondary lymphedema.
    Intervention Description
    Unstable shoes were compared with conventional sports shoes, the objective being to evaluate possible differences in the evolution of lymphedema. During a clinical trial lasting eight weeks, we assessed quality of life, limb volume, and symptoms derived from lymphedema.
    Primary Outcome Measure Information:
    Title
    Volume of the lower limb
    Description
    Volume of the lower limb
    Time Frame
    8 weeks
    Secondary Outcome Measure Information:
    Title
    Circumference measure of the foot
    Description
    Circumference measure of the foot
    Time Frame
    8 weeks
    Title
    Changes in lymphedema symptoms
    Description
    Changes in lymphedema symptoms
    Time Frame
    8 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: -Subjects affected with lower limb lymphedema -primary, secondary, unilateral or bilateral-, -Daily use of a compression stocking Exclusion Criteria: Subjects with acute infection of the affected limb that did not had any treatment for lymphedema one year prior to the study, Weight <40kg, shoe size <EU35 or >EU47 that have previously used unstable shoes vestibular alterations, vertigo, hypoacusis visual compromise that affects balanc

    12. IPD Sharing Statement

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    Use of the Unstable Shoes in Lower Limb Lymphedema.

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