Skip to main content
Clinical Trials/NCT03961412
NCT03961412
Unknown
Early Phase 1

Evaluation of A Family-based Intervention to Improve Pap Test Screening Among Under-screened Chinese American Immigrant Women

University of Nevada, Reno0 sites224 target enrollmentJuly 2022

Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Cervical Cancer
Sponsor
University of Nevada, Reno
Enrollment
224
Primary Endpoint
Change in Receiving a Pap Test
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to find out the impact of the involvement of an influential person(s) (e.g., spouse, partners, parents, children, friends) on Pap test screening intention and behaviors, Pap test self-efficacy, and perceived benefits and barriers to Pap test screening among Chinese American immigrant women. These data specific to the impact of the involvement of an influential person on Pap test screening could be used to develop successful cancer prevention programs that target the specific needs of Chinese populations.

Detailed Description

The importance of the support from family, spouse, friends, or significant others has been noted among Chinese American immigrant women (CAIW), but little attention has been paid to the effects of family-based (FB) interventions, especially for cervical cancer screening. Understanding the role of CAIW's family in promoting Pap screening and other influences can lead to the creation of more culturally appropriate screening interventions. The objective of this study is to test the effects of a FB intervention on Pap test intention and behaviors, Pap test self-efficacy, and perceived benefits and barriers to Pap tests among under-screened CAIW aged 21-65. This pilot test of the FB intervention will be conducted using a randomized controlled design with two groups only, experimental and control groups. Interventions will be delivered by bilingual and bicultural CAIW trained facilitators. Post-test and follow-up telephone surveys will be conducted at 2 weeks and 6 months after the intervention.

Registry
clinicaltrials.gov
Start Date
July 2022
End Date
June 2024
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wei-Chen Tung

Associate Professor, PhD, RN, FAAN

San Jose State University

Eligibility Criteria

Inclusion Criteria

  • a first-generation Chinese American
  • no previous cervical cancer screening within the past 3 years
  • no total hysterectomy
  • no history of cervical cancer
  • able to read English, Simple Chinese, or Traditional Chinese.

Exclusion Criteria

  • Not a Chinese American immigrant
  • Had total hysterectomy
  • Had history of cervical cancer
  • Not able to read English or Chinese

Outcomes

Primary Outcomes

Change in Receiving a Pap Test

Time Frame: 6 months after intervention

Change from baseline in use of a Pap test 6 months after intervention

Change in Intention to Receive a Pap Test

Time Frame: 6 months after intervention

Change from baseline in intention to receive a Pap test 6 months after intervention

Similar Trials