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A Pap Test Intervention to Enhance Decision Making Among Pacific Islander Women

C

California State University, Fullerton

Status

Completed

Conditions

Cervical Cancer

Treatments

Behavioral: Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03064581
CSUFR01CA149324
R01CA149324 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This community-based randomized trial tested the effects of a social support intervention to increase Chamorro, Samoan, and Tongan women's Pap test behavior and social support among their male spouses or significant others in Southern California.

Full description

The purpose of this five-year community-based randomized trial was to: 1) examine the Pap test decision making process in Pacific Islander women; 2) assess the role of social support within the decision making process; and 3) develop and test an intervention to increase Pap testing among Pacific Islander women, and support among their male spouses/significant others. The intervention was created utilizing a Multi-Attribute Utility model and social support theory resulting in gender-specific educational workshops consisting of a social support intervention that informed both Pacific Islander women and men about cervical cancer and the importance of Pap testing for Pacific Islander women, and aimed to increase social support among their male spouses/significant others.

Enrollment

1,014 patients

Sex

All

Ages

21 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women ages 21 to 65
  • Of Chamorro, Samoan, and/or Tongan ethnicity
  • Has a significant other (married or in a long-term relationship for more than 5 years).

Exclusion criteria

  • Not a member of one of the churches or clans visited for recruitment

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,014 participants in 2 patient groups

Intervention
Experimental group
Description:
Gender-specific culturally tailored social-support informed educational intervention session.
Treatment:
Behavioral: Intervention
Control
No Intervention group
Description:
Usual care with delayed intervention at the end of study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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