Breast Cancer Screening Intervention
|ClinicalTrials.gov Identifier: NCT01525264|
Recruitment Status : Completed
First Posted : February 2, 2012
Last Update Posted : August 18, 2016
|Condition or disease||Intervention/treatment|
|Breast Cancer||Behavioral: KIM-CHI Behavioral: Healthy Wife Control Group|
Show Detailed Description
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||434 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Korean Immigrants & Mammography—Culture-Specific Health Intervention (KIM-CHI)|
|Study Start Date :||August 2008|
|Primary Completion Date :||September 2010|
|Study Completion Date :||October 2010|
Experimental: Culturally Relavent Education
Education about improving diet using a DVD with Korean role models and native Korean language.
The intervention is based on cultural characteristics and context and focuses on changing (1) beliefs about breast cancer and screening, (2) knowledge of breast cancer and screening, (3) self-efficacy of confidence in one's ability to complete all the steps necessary for obtaining a mammogram including requesting a referral for mammogram from a physician. The KIM-CHI program also incorporates strategies for enhancing spousal support (perceived support received from husband). To standardize delivery of culture-relevant health behavior change information related to breast cancer screening to groups of women and their husbands separately, the KIM-CHI program uses a DVD with Korean role models, native Korean language, and male physician authentication as well as inclusion of spouses.
Other Name: Culturally relavent intervention
Active Comparator: Healthy Wife Intervention
Intervention group of couples who received education about importance of a Healthy Diet. It was an attention control group
Behavioral: Healthy Wife Control Group
Intervention group of couples who received education about importance of Healthy diet
Other Name: Healthy Diet
- Change from baseline in mammography uptake at 15 months [ Time Frame: 6- and 15-months post-baseline ]Non of the participants at baseline had a mammogram within the previous 1 year. The primary outcome was measured by self-report about how many times and when (month and year) mammograms were obtained by women in the study, with follow-up validation by the mammography facility for each woman who reports having had a mammogram in the past 15 months at Time 3. The number of mammograms (o, 1, or 2) and length of time to mammogram were calculated.
- Health beliefs [ Time Frame: 6- and 15-months post-baseline ]health beliefs (perceived seriousness, susceptibility, benefits, barriers, knowledge, self-efficacy about breast cancer and screening) were measured by using Likert-type scale, ranging from strongly disagree = 1 to strongly agree = 5.
- Spousal Support [ Time Frame: 6- and 15-months post-baseline ]Women's perceived spousal support received from husbands and husbands' perceived spousal support provided to their wives were measured.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01525264
|Principal Investigator:||Eunice E Lee, PhD||UCLA School of Nursing|