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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01686737
Other study ID # 2012210
Secondary ID
Status Withdrawn
Phase N/A
First received September 12, 2012
Last updated February 4, 2013
Start date November 2012
Est. completion date July 2014

Study information

Verified date February 2013
Source Universität Duisburg-Essen
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

Breast cancer is the most frequent cancer in women and is associated with profound restrictions of health-related quality of life and psychosocial health. More than three-quarters of women with breast cancer suffer from fatigue during cancer treatment. While exercise interventions can improve fatigue in breast cancer patients, many patients request complementary treatment approaches. Therefore, this study investigates the effects of yoga in women with breast cancer compared to aerobic exercise and usual care.

It is hypothesized that yoga is more effective than usual care and equally effective as aerobic exercise.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- non-metastatic invasive breast cancer

- currently receiving adjuvant chemotherapy

- moderate to severe chemotherapy-induced fatigue

- physical and cognitive capacity to participate in yoga or walking

Exclusion Criteria:

- diagnosed and pharmacologically treated psychiatric disorder except depressive adaptation disorder as a reaction to cancer diagnosis

- ECOG status > 1

- prior malignancy with a disease-free survival < 10 years except curatively treated basalioma of the skin and carcinoma in situ of the cervix

- prior ductal carcinoma in situ (DCIS) ot the breast

- pregnancy or breastfeeding

- regular practice of yoga or walking during the past 12 months

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Iyengar Yoga
12 weeks of Iyengar yoga 2 weekly sessions of 60 minutes
Walking
12 weeks of walking 2 weekly sessions of 60 minutes

Locations

Country Name City State
Germany Klinik für Senologie / Brustzentrum, Kliniken Essen-Mitte Essen
Germany Brustzentrum Köln-Hohenlind, St. Elisabeth-Krankenhaus Köln-Hohenlind Köln

Sponsors (1)

Lead Sponsor Collaborator
Universität Duisburg-Essen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fatigue Multidimensional Fatigue Inventory Week 12 No
Secondary Fatigue Multidimensional Fatigue Inventory Week 36 No
Secondary Health-related quality of life Functional Assessment of Cancer Therapy - Breast Week 12, week 36 No
Secondary Depression and anxiety Hospital Anxiety and Depression Scale Week 12, week 36 No
Secondary Sleep quality Pittsburgh Sleep Quality Index Week 12, week 36 No
Secondary Perceived Stress Perceived Stress Scale
Impact of Event Scale
Week 12, week 36 No
Secondary Salivary Cortisol Cortisol awakening response Week 12, week 36 No
Secondary Safety Adverse events Week 0-36 Yes
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