Determining Quality of Life in Breast Cancer Patient After Completing Radiation,Chemotherapy,Surgery or Combination

PHASE2WithdrawnINTERVENTIONAL
Enrollment

460

Participants

Timeline

Start Date

February 28, 2010

Primary Completion Date

February 28, 2014

Study Completion Date

February 28, 2014

Conditions
Breast Carcinoma
Interventions
BEHAVIORAL

Counseling

• Arm II: Patients receive audio visual aids and weekly counseling sessions by the expert counselors and breast cancer survivors over 8 weeks for a total of 8-16 sessions. Patients receive written materials from the counseling group after the completion of the sessions

BEHAVIORAL

Written materials

• Arm I: Patients receive the support by providing existing resources. Patients receive standard written materials from the counseling group after enrolling in the study.

Trial Locations (1)

07726

Practicing physician in New Jersey, Englishtown

Sponsors
All Listed Sponsors
lead

American Scitech International

OTHER

NCT00712621 - Determining Quality of Life in Breast Cancer Patient After Completing Radiation,Chemotherapy,Surgery or Combination | Biotech Hunter | Biotech Hunter