Post-treatment Care of Breast Cancer Survivors

Status Completed

Clinical Trial Summary

The overall goal of this proposal is to improve the post-treatment care of breast cancer survivors and to understand the barriers to optimal post-treatment care in Latina and Non-Hispanic women.

Clinical Trial Description

The proposed investigation is a randomized prospective evaluation of a Survivorship Intervention in improving the quality of care, treatment satisfaction and understanding of care in Latina and Caucasian breast cancer survivors treated in an urban academic medical center. Patients will be recruited within 6 weeks of completing their last definitive breast cancer therapy (radiation or chemotherapy). Patients will complete self administered baseline and follow-up questionnaires. Following baseline evaluation patients will be randomized to receiving either written information for follow-up care of cancer survivors published by the National Cancer Institute (Facing Forward), or the Survivorship Intervention. Patients will not be aware that they are participating in a randomized intervention. After verbally agreeing to participate they will be randomized to group A or B and will receive the corresponding consent. Patients will be re-assessed 3 and 6 months after enrollment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00821288
Study type	Interventional
Source	Columbia University
Contact
Status	Completed
Phase	N/A
Start date	July 2007
Completion date	May 2013

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT03273426` - Prediction of pCR by Preoperative Biopsy in Breast Cancer With cCR After Neoadjuvant Chemotherapy.	N/A
Recruiting	`NCT04583124` - Adjusting the Dose of Therapeutic Exercise to Prevent Neurotoxicity Due to Anticancer Treatment (ATENTO)	N/A
Active, not recruiting	`NCT04489173` - TAS102 in Patients With ER-positive, HER2-negative Advanced Breast Cancer	Phase 2
Recruiting	`NCT02913573` - Effect of Pectoral Nerve Block on Post-op Pain in Patients Undergoing Mastectomy and Immediate Reconstruction	Phase 2
Completed	`NCT03124095` - Combined Training Intervention for Women Who Underwent Primary Treatment for Breast Cancer	N/A
Terminated	`NCT00251095` - Comparison of Safety and Efficacy of TOCOSOL(R) Paclitaxel Versus Taxol(R) for Treatment of Metastatic Breast Cancer	Phase 3
Completed	`NCT05576545` - Develop and Evaluate the Effectiveness of a Self-Care Smartphone Application on the Self-Efficacy, and Resilience Among Newly Diagnosed Breast Cancer Patients Undergoing Treatment	N/A
Active, not recruiting	`NCT03625635` - Effect of a Clinical Nutrition Intervention Program in Breast Cancer Patients During Antineoplastic Treatment	N/A
Recruiting	`NCT04799535` - Quantitative Microvasculature Imaging for Breast Cancer Detection and Monitoring
Withdrawn	`NCT03266562` - Estrogen Receptor Expression in Breast Cancer - Assessed With Positron Emission Mammography	N/A
Completed	`NCT00530868` - Comparing Letrozole Given Alone to Letrozole Given With Avastin in Post-Menopausal Women Breast Cancer	Phase 2
Recruiting	`NCT06255808` - Development of Assist Tool for Breast Examination Using the Principle of Ultrasonic Sensor
Completed	`NCT04640220` - Improvement of Range of Motion in Frozen Shoulder in Breast Cancer Survivors	N/A
Completed	`NCT02970682` - SFX-01 in the Treatment and Evaluation of Metastatic Breast Cancer	Phase 2
Completed	`NCT02316561` - Single Dose Ablative Radiation Treatment for Early-Stage Breast Cancer	N/A
Terminated	`NCT00638963` - Temozolomide as a Prophylaxis Against Brain Recurrence in Participants With Metastatic Breast Cancer (P05225 AM2)	Phase 2
Terminated	`NCT00249301` - A Study of MLN8054 in Patients With Advanced Solid Tumors	Phase 1
Not yet recruiting	`NCT06056414` - Study of Anxiety After a Session of Energy Resonance by Cutaneous Stimulation	N/A
Recruiting	`NCT05427071` - Magnetic Marker Localization for Occult Breast Cancer and Target Axillary Dissection in Node-positive Breast Cancer Post-neoadjuvant Chemotherapy	N/A
Recruiting	`NCT03740893` - PHOENIX DDR/Anti-PD-L1 Trial: A Pre-surgical Window of Opportunity and Post-surgical Adjuvant Biomarker Study of DNA Damage Response Inhibition and/or Anti-PD-L1 Immunotherapy in Patients With Neoadjuvant Chemotherapy Resistant Residual Triple Negative Breast Cancer	Phase 2