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NCT01612338 · ClinicalTrials.gov registry record · NA

Interventions to Increase Screening by Breast Cancer Survivors and Their High Risk Female Relatives

A NA study of Breast Cancer and Breast Cancer in Young Women, sponsored by University of Michigan.

Completed
Registry status
NA
Development phase
1,290
Enrollment target
2
Study locations

NCT01612338: Completed NA study of Breast Cancer and Breast Cancer in Young Women, sponsored by University of Michigan.

NCT01612338 is a NA study of Breast Cancer and Breast Cancer in Young Women that has completed, run by University of Michigan. The registered enrollment target is 1,290 participants, below the 2,802-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (54% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01612338, a NA study of Breast Cancer and Breast Cancer in Young Women, has completed, sponsored by University of Michigan.

COMPLETED
Registry status
NA
Development phase
1,290 participants
Enrollment target
2
Study locations

Study Summary

The University of Michigan (UM) Schools of Nursing, Public Health, and Medicine, the Michigan Department of Community Health (MDCH) and the Michigan Cancer Consortium (MCC) are conducting a multidisciplinary academic/practice three-year project to increase appropriate breast cancer screening for young breast cancer survivors and their cancer-free, female relatives at greatest risk for breast cancer. The aims of this project are to: 1) identify and survey 3000 breast cancer survivors reported to the Michigan Cancer Surveillance Program who were diagnosed between the ages of 20-45 years regarding their breast cancer screening utilization; 2) identify and survey the survivors' female relatives regarding their breast cancer screening utilization; and 3) implement two versions (targeted vs. enhanced tailored) of an evidence-based intervention recommended by the Guide to Community Preventive Services to increase breast cancer screening. A follow-up survey will assess the effectiveness of each intervention on a) breast cancer screening utilization; b) perceived barriers and facilitators to screening; c) self-efficacy in utilizing screening services; d) family support related to screening; e) knowledge of the genetics of breast cancer and personal risk factors; and f) satisfaction with the intervention.

Primary Outcome

self report of mammogram and clinical breast exam

Interventions

  • BEHAVIORAL Targeted
  • BEHAVIORAL Enhanced Tailored

Study Locations (2)

Michigan

  • University of Michigan School of Nursing - Ann Arbor
  • Michigan Department of Community Health - Lansing

Trial Details

FieldValue
Enrollment Target 1,290 participants
Start Date 2012-07
Est. Completion 2014-09
Phase NA
University of Michigan

1,327 total trials

What the finished NCT01612338 record still lists

NCT01612338 is an interventional study that assigns participants to a tested intervention. Its 1,290 participants enrollment target places it among the larger protocols in the corpus, below the 2,802-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (54% lower).

The record links to 3 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which Targeted is the first listed.

NCT01612338 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT01612338 about?

NCT01612338 is a clinical study titled "Interventions to Increase Screening by Breast Cancer Survivors and Their High Risk Female Relatives". The University of Michigan (UM) Schools of Nursing, Public Health, and Medicine, the Michigan Department of Community Health (MDCH) and the Michigan Cancer Consortium (MCC) are conducting a multidisciplinary academic/practice three-year project to increase appropriate breast cancer screening for you...

What is the current status of trial NCT01612338?

This trial is currently completed. It is a NA study. The enrollment target is 1,290 participants. The study started on 2012-07. Estimated completion is 2014-09.

What conditions does trial NCT01612338 study?

This clinical trial studies the following conditions: Breast Cancer, Breast Cancer in Young Women, Breast Cancer in Women With a Strong Family History.

What interventions are being tested in trial NCT01612338?

The interventions under investigation include: Targeted (BEHAVIORAL), Enhanced Tailored (BEHAVIORAL).

Who is sponsoring clinical trial NCT01612338?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01612338 being conducted?

This trial has 2 study locations across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Breast Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01612338's enrollment target sits among peer trials

1,290 95th of 1224 higher than 1,130 of 1,224 other Breast Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Breast Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01612338, the US trial registry maintained by the National Library of Medicine. NCT01612338 (large enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.