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Effects of a Videogame-based Program on Women With Lymphedema Secondary to Breast Cancer

N/ACompletedNCT02958332
Universidad de Burgos11 enrolled

Overview

Aims: To demonstrate the effect of a program based on video games as a means to improve abilities and basic skills affected by lymphedema, and its impact on quality of life. Design: longitudinal, pre-experimental, with pre / post-test and evaluation, assessor blinded study. Method: Data on shoulder pain and disability, health-related quality of life, strength and articulate activated by the OSS (Oxford Shoulder Score), SPADI (Shoulder Pain and Disability Index), FACT-B + 4 (Functional Assesment of Cancer Therapy Questionnaire for Breast Cancer), respectively goniometry and dynamometry amplitude scales will be collected. The intervention will be performed with the Wii ™ console and the Wii Balance BoardTM, during 5 individual weekly sessions of 30 minutes.

Study Type

INTERVENTIONAL

Allocation

NA

Purpose

TREATMENT

Masking

NONE

Enrollment

11

Conditions

LymphedemaBreastcancer

Interventions

video game programOTHER

Participants will use the Wii console and the Wii balance board, to play different video games which imply shoulder movements. They will receive 5 individual sessions of 30 minutes.

Eligibility

Sex: ALLMin age: 18 Years
Medical Language ↔ Plain English
Inclusion Criteria: * Be over 18 years * Have a diagnosis of lymphedema, secondary to breast cancer Exclusion Criteria: * Stage 0 or subclinical lymphedema * Present other shoulder pathology apart from lymphedema

Locations (1)

Universidad de Burgos. Facultad de Ciencias de la Salud.

Burgos, Spain

Outcomes

Primary Outcomes

Change in Range motion

Time frame: Pre intervention and one week after having finished the program

Change in strength

Time frame: Pre intervention and one week after having finished the program

Change in Oxford Shoulder Scale

Time frame: Pre intervention and one week after having finished the program

Change in Shoulder Pain and Disability Index

Time frame: Pre intervention and one week after having finished the program

Secondary Outcomes

Change in quality of life (FUNCTIONAL ASSESMENT OF CANCER THERAPY QUESTIONNAIRE FOR BREAST CANCER (FACT-B+4)

Time frame: Pre intervention and one week after having finished the program

Data from ClinicalTrials.gov

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