Breast Neoplasms Clinical Trial
— IFaBOfficial title:
Iyengar Yoga for Chemotherapy-induced Fatigue in Breast Cancer Patients
Verified date | February 2013 |
Source | Universität Duisburg-Essen |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Ethics Commission |
Study type | Interventional |
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.
Status | Withdrawn |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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | Klinik für Senologie / Brustzentrum, Kliniken Essen-Mitte | Essen | |
Germany | Brustzentrum Köln-Hohenlind, St. Elisabeth-Krankenhaus Köln-Hohenlind | Köln |
Lead Sponsor | Collaborator |
---|---|
Universität Duisburg-Essen |
Germany,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
NCT05558917 -
Comparison Between PECS BLOCK 2 vs ESP BLOCK in Ocnologic Breast Surgery
|
N/A | |
Active, not recruiting |
NCT03664778 -
Abbreviated Breast MRI After Cancer Treatment
|
||
Recruiting |
NCT03144622 -
18F-FSPG PET/CT Imaging in Patients With Cancers
|
||
Completed |
NCT05452499 -
Pain Neuroscience Education and Therapeutic Exercise as a Treatment for Breast Cancer Survivors Living With Sequelae
|
N/A | |
Active, not recruiting |
NCT04568902 -
Study of H3B-6545 in Japanese Women With Estrogen Receptor (ER)-Positive, Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Breast Cancer
|
Phase 1 | |
Completed |
NCT02860585 -
Evaluation of Survival in Patients With Metastatic Breast Cancer Receiving High-dose Chemotherapy With Autologous Haematopoietic Stem Cell Transplantation
|
N/A | |
Completed |
NCT04059809 -
Photobiomodulation for Breast Cancer Radiodermatitis
|
Phase 2/Phase 3 | |
Recruiting |
NCT04557449 -
Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors
|
Phase 1/Phase 2 | |
Completed |
NCT03698942 -
Delphinus SoftVueâ„¢ ROC Reader Study
|
||
Completed |
NCT00092950 -
Exercise in Women at Risk for Breast Cancer
|
Phase 2 | |
Terminated |
NCT04123704 -
Sitravatinib in Metastatic Breast Cancer
|
Phase 2 | |
Not yet recruiting |
NCT02151071 -
The Breast Surgery EnLight and LightPath Imaging System Study
|
Phase 1/Phase 2 | |
Recruiting |
NCT02934360 -
TR(ACE) Assay Clinical Specimen Study
|
N/A | |
Active, not recruiting |
NCT02950064 -
A Study to Determine the Safety of BTP-114 for Treatment in Patients With Advanced Solid Tumors With BRCA Mutations
|
Phase 1 | |
Not yet recruiting |
NCT02876848 -
A Novel E-Health Approach in Optimizing Treatment for Seniors (OPTIMUM Study)
|
N/A | |
Completed |
NCT02931552 -
Nuevo Amanecer II: Translating a Stress Management Program for Latinas
|
N/A | |
Recruiting |
NCT02547545 -
Breast Cancer Chemotherapy Risk Prediction Mathematical Model
|
N/A | |
Completed |
NCT02518477 -
Preventive Intervention Against Lymphedema After Breast Cancer Surgery
|
N/A | |
Completed |
NCT02652975 -
Anticancer Treatment of Breast Cancer Related to Cardiotoxicity and Dysfunctional Endothelium
|
N/A | |
Completed |
NCT02303366 -
Pilot Study of Stereotactic Ablation for Oligometastatic Breast Neoplasia in Combination With the Anti-PD-1 Antibody MK-3475
|
Phase 1 |