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Developing a Self-persuasion Intervention Promoting Adolescent HPV Vaccination

Not Applicable
Completed
Conditions
Human Papillomavirus Vaccines
Interventions
Behavioral: Project Voice
Registration Number
NCT02537756
Lead Sponsor
University of Texas Southwestern Medical Center
Brief Summary

HPV vaccine coverage among adolescents in the US is suboptimal. This is particularly true among traditionally underserved adolescents. Few parent-targeted interventions have focused on the parental decision-making process. Self-persuasion, generating one's own arguments for engaging in a behavior, may be an effective means to influence parents' motivation to vaccinate their children. In a three-phase study, investigators are using quantitative and qualitative research methods to develop and refine a tablet-based self-persuasion intervention for parents who are undecided about the HPV vaccine. This clinical trial submission focuses on the second phase of the study. The results of the second phase will inform the third phase of the trial (also registered in clinical trials).

Detailed Description

Despite the fact that HPV vaccination is recommended for male and female adolescents, HPV vaccine 3 dose coverage among adolescents is poor (38% for girls, 14% for boys). HPV-related cancers are a significant burden on the US healthcare system and could be prevented through adolescent vaccination. Rates of vaccination are suboptimal among underserved populations (uninsured, low-income, racial and ethnic minorities) often seen in safety-net clinics. Few interventions have been designed that target decision-making among parents of unvaccinated adolescents. Self-persuasion, generating of one's own arguments for a health behavior, may be an effective means of influencing HPV vaccination behaviors among undecided or ambivalent parents. Through three stages, investigators will identify and develop a self-persuasion intervention strategy to promote adolescent HPV vaccination in safety-net clinics. The current trial, Stage 2, is a four-arm randomized controlled trial (RCT), using a 2x2 factorial design, in which investigators will assign participants to one of four self-persuasion intervention conditions that vary by cognitive processing level (verbalize vs. listen to arguments) and choice of argument topics (parents choose vs. are assigned topics) to identify which intervention condition is optimal. Conducted in a laboratory setting, investigators will identify and select the optimal intervention condition through quantitative analysis of the effects on parents' vaccination intentions and qualitatively by exploring parental experiences with the self-persuasion tasks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
737
Inclusion Criteria
  • Undecided parents (18 years and older) whose children are 11-17 year old patients who have not begun the HPV vaccine series.
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Exclusion Criteria
  • Parents whose child is a pregnant adolescent
  • Lack telephone access
  • Having impairing hearing or speech
  • Participants will be excluded from participation in future stages
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
3- Verbalize, AssignedProject VoiceParents will use a tablet-based application (Project Voice) that directs them to verbalize their own arguments based on topics assigned to them
1- Verbalize, ChoiceProject VoiceParents will use a tablet-based application (Project Voice) that directs them to verbalize their own arguments based on topics they choose
2- Listen, ChoiceProject VoiceParents will use a tablet-based application (Project Voice) that directs them to listen to peer-generated arguments based on topics they choose
4- Listen, AssignedProject VoiceParents will use a tablet-based application (Project Voice) that directs them to listen to peer-generated arguments based on topics assigned to them
Primary Outcome Measures
NameTimeMethod
Survey Items Measuring Parental Intentions to vaccinateDuring the intervention visit (1 hr)

Change in intentions of the parent to vaccinate from baseline survey to exit survey using measures adapted from Gerend \& Shepherd (2012). Intentions Likert Scale responses range from 1-very likely to 5-very unlikely.

Secondary Outcome Measures
NameTimeMethod
HPV vaccination behavior documented in the electronic medical record, initiation12 months

Number of parents who initiated the series by vaccinating their child within 12 months of the study appointment as evidenced by documentation in the child's electronic medical record.

Change in Decision StageDuring the intervention visit (1 hr)

Change in decision stage response of parents from baseline survey to post-educational video to post-intervention tasks.

Trial Locations

Locations (1)

UT Southwestern Medical Center

🇺🇸

Dallas, Texas, United States

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