Effects of Complex Decongestive Therapy Applied on Patients With Lower Extremity Lymphedema

NCT ID: NCT05239273

Last Updated: 2022-02-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-31

Study Completion Date

2023-03-31

Brief Summary

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The aim of this study is to investigate the effects of complex decongestive therapy applied to patients with lymphedema in the lower extremities on body awareness, functionality and quality of life.

Detailed Description

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Lymphedema is a chronic condition characterized by the permanent accumulation of protein-rich fluid in certain body regions as a result of the dysfunction of the lymphatic system, in which skin and subcutaneous changes are added to the picture. Pain in the affected extremity and other accompanying lymphedema symptoms can negatively affect functionality and quality of life, and swelling in the extremity can negatively affect the body image of individuals. Today, Complex Decongestive Therapy (CDT) is accepted as the gold standard in the treatment of lymphedema. It has been shown in the literature that CDT has positive effects on parameters such as functionality, quality of life, and balance in patients with upper limb lymphedema. There are few studies investigating the effects of CDT on body awareness, functionality and quality of life in patients who developed lymphedema in the lower extremities.

Conditions

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Lymphedema

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Complex Decongestive Therapy (CDT) Group

Phase 1 of CDT will be applied to CDT group. This application consists of manual lymph drainage, skin care, compression bandage and exercises. This phase will continue 5 days a week for 3 weeks.

Group Type EXPERIMENTAL

Complex Decongestive Therapy

Intervention Type OTHER

Phase 1 of CDT will be applied. This application consists of manual lymph drainage, skin care, compression bandage and exercises.

Control group

Waiting list will included in control group.

Group Type OTHER

Control

Intervention Type OTHER

No intervention

Interventions

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Complex Decongestive Therapy

Phase 1 of CDT will be applied. This application consists of manual lymph drainage, skin care, compression bandage and exercises.

Intervention Type OTHER

Control

No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Be between the ages of 18-65
* Having unilateral lymphedema in the lower extremity
* Volunteer to participate in the study

Exclusion Criteria

* Having bilateral lower extremity lymphedema
* Having an active infection
* Having a mental cognitive disorder
* Being unable to communicate and cooperate
* Conditions where manual lymphatic drainage is contraindicated (such as severe heart failure and/or uncontrolled rhythm disturbance, uncontrollable hypertension, being pregnant, presence of thrombus, active infection ect.)
* Presence of metastases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ankara Yildirim Beyazıt University

OTHER

Sponsor Role lead

Responsible Party

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seyda toprak celenay

associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Seyda Toprak Celenay

Role: PRINCIPAL_INVESTIGATOR

Ankara Yildirim Beyazıt University

Central Contacts

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Seyda Toprak Celenay

Role: CONTACT

+90312 906 1000

Other Identifiers

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2022/02/05

Identifier Type: -

Identifier Source: org_study_id

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