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A Lifestyle Intervention for Breast Cancer Survivors

NCT01819324 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 173

Last updated 2015-12-03

No results posted yet for this study

Summary

1. The purpose of the study is to test the effectiveness of a new mail-based intervention for breast cancer survivors compared with standard lifestyle management and no-treatment.
2. This intervention addresses both lifestyle factors such as dietary and physical activities and psychological issues specific to breast cancer survivors to improve healthy behaviors.

Conditions

Interventions

BEHAVIORAL

Targeting the Teachable Moment

TTMI material (every other week for 4 months)

BEHAVIORAL

Standardized Lifestyle Management

SLM material (every other week for 4 months)

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • Hartford Hospital

    lead OTHER

Principal Investigators

  • Crystal L. Park, Ph.D · University of Connecticut

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2013-11-30
Completion
2015-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01819324 on ClinicalTrials.gov