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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03205969
Other study ID # C2014147
Secondary ID
Status Completed
Phase N/A
First received June 29, 2017
Last updated June 29, 2017
Start date January 5, 2015
Est. completion date December 31, 2015

Study information

Verified date June 2017
Source Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether functional games can be used to improve the adherence and quality of life of breast cancer patients with chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 31, 2015
Est. primary completion date December 31, 2015
Accepts healthy volunteers No
Gender All
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- Diagnosed with breast cancer

- Receiving breast cancer chemotherapy

- Patients who are using a smartphone and agree to use a mobile functional game

Exclusion Criteria:

- Patient with intellectual disability

- Diagnosed with congenital genetic disease

- Patients with a history of acquired brain injury such as cerebral palsy

- Developmental disorders, including autism

- Patients with language or learning disabilities

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Functional mobile game
Functional mobile game for chemotherapy side effect education

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Chung-Ang University Hosptial, Chung-Ang University College of Medicine

References & Publications (7)

Beutel ME, Weißflog G, Leuteritz K, Wiltink J, Haselbacher A, Ruckes C, Kuhnt S, Barthel Y, Imruck BH, Zwerenz R, Brähler E. Efficacy of short-term psychodynamic psychotherapy (STPP) with depressed breast cancer patients: results of a randomized controlled multicenter trial. Ann Oncol. 2014 Feb;25(2):378-84. doi: 10.1093/annonc/mdt526. Epub 2013 Dec 16. — View Citation

Carayol M, Romieu G, Bleuse JP, Senesse P, Gourgou-Bourgade S, Sari C, Jacot W, Sancho-Garnier H, Janiszewski C, Launay S, Cousson-Gélie F, Ninot G. Adapted physical activity and diet (APAD) during adjuvant breast cancer therapy: design and implementation of a prospective randomized controlled trial. Contemp Clin Trials. 2013 Nov;36(2):531-43. doi: 10.1016/j.cct.2013.09.016. Epub 2013 Oct 4. — View Citation

DeNysschen CA, Burton H, Ademuyiwa F, Levine E, Tetewsky S, O'Connor T. Exercise intervention in breast cancer patients with aromatase inhibitor-associated arthralgia: a pilot study. Eur J Cancer Care (Engl). 2014 Jul;23(4):493-501. doi: 10.1111/ecc.12155. Epub 2013 Dec 2. — View Citation

Hwang SY, Chang SJ, Park BW. Does chemotherapy really affect the quality of life of women with breast cancer? J Breast Cancer. 2013 Jun;16(2):229-35. doi: 10.4048/jbc.2013.16.2.229. Epub 2013 Jun 28. — View Citation

Jung KW, Won YJ, Kong HJ, Oh CM, Seo HG, Lee JS. Cancer statistics in Korea: incidence, mortality, survival and prevalence in 2010. Cancer Res Treat. 2013 Mar;45(1):1-14. doi: 10.4143/crt.2013.45.1.1. Epub 2013 Mar 31. — View Citation

Segrin C, Badger TA. Psychological and physical distress are interdependent in breast cancer survivors and their partners. Psychol Health Med. 2014;19(6):716-23. doi: 10.1080/13548506.2013.871304. Epub 2014 Jan 2. — View Citation

Touillaud M, Foucaut AM, Berthouze SE, Reynes E, Kempf-Lépine AS, Carretier J, Pérol D, Guillemaut S, Chabaud S, Bourne-Branchu V, Perrier L, Trédan O, Fervers B, Bachmann P. Design of a randomised controlled trial of adapted physical activity during adjuvant treatment for localised breast cancer: the PASAPAS feasibility study. BMJ Open. 2013 Oct 28;3(10):e003855. doi: 10.1136/bmjopen-2013-003855. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary International Physical Activity Questionnaires (IPAQ) To obtain comparable estimates of physical activity overall assessment period (3 weeks)
Secondary Beck Depression Inventory (BDI) overall assessment period (3 weeks)
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