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OpenTrials
Completed

NCT Number: NCT00742755

Increasing Adherence to Follow-up of Breast Abnormalities in Low-Income Korean American Women

Develop and evaluate a peer navigator intervention to assist Korean women with a potential breast abnormality, who have missed their first follow-up appointment, to complete all diagnostic follow-up tests.

Completed

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Key information

Age range

40 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Division of Cancer Prevention and Control Research, University of California Los Angeles

Los Angeles, California, 90095-6900, United States

About this study

The purpose of this study is to design an intervention to assist Korean American women who have been identified with a potential breast abnormality through the Breast Cancer Early Detection Program and who have missed their first follow-up appointment (at risk women). Intervention activities will include reminder phone calls or home visits by a trained peer navigator to explain the importance of follow-up procedures, emotional support, help with transportation to follow-up appointments, translations, organizing care for children or grandchildren during medical appointments, and other assistance to overcome barriers to follow-up identified during the initial phase of the study. The investigators will collect extensive process measures including number and type of intervention activities requested and delivered in order to estimate the feasibility for institutionalizing intervention activities. The investigators will conduct chart reviews and a follow-up survey to evaluate the effectiveness of the intervention in increasing adherence to follow-up procedures.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being: a Korean American woman
  • Screened through the Breast Cancer Early Detection Program
  • With a potential breast abnormality
  • Having missed a first diagnostic follow-up appointment

Exclusion criteria

  • Not a Korean American woman
  • Not screened through the Breast Cancer Early Detection Program
  • No potential breast abnormality
  • Not having missed a first diagnostic follow-up appointment

Treatment and study plan

Prospective intervention

Behavioral

Prospective Intervention: Peer navigator who assists with appointment making, transportation, translations, completing forms, etc.

Other names: Intervention group

Primary outcomes

  1. Completion of all recommended follow-up tests

    Time frame: 6 months post-intervention

Secondary outcomes

  1. Time to completion

    Time frame: 6 months post-intervention

Sponsors and collaborators

Lead sponsor

Jonsson Comprehensive Cancer Center

Other

Collaborators

  • U.S. Army Medical Research and Development Command

Registry information

Important dates

Study start
2003
Primary completion
2009
Study completion
2009
First posted
Aug 28, 2008
Registry last updated
Aug 19, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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