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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02958332
Other study ID # CB-MSV-19-09-2016
Secondary ID
Status Completed
Phase N/A
First received October 28, 2016
Last updated May 3, 2017
Start date November 2016
Est. completion date January 2017

Study information

Verified date May 2017
Source Universidad de Burgos
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date January 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
video game program
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.

Locations

Country Name City State
Spain Universidad de Burgos. Facultad de Ciencias de la Salud. Burgos

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Burgos

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Range motion Pre intervention and one week after having finished the program
Primary Change in strength Pre intervention and one week after having finished the program
Primary Change in Oxford Shoulder Scale Pre intervention and one week after having finished the program
Primary Change in Shoulder Pain and Disability Index Pre intervention and one week after having finished the program
Secondary Change in quality of life (FUNCTIONAL ASSESMENT OF CANCER THERAPY QUESTIONNAIRE FOR BREAST CANCER (FACT-B+4) Pre intervention and one week after having finished the program
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