Investigating Facilitator-driven, Multi-level Implementation Strategies in Federally Qualified Health Centers to Improve Provider Recommendation and HPV Vaccination Rates Among Latino/a Adolescents
Purpose
The purpose of this study is to determine the provider- and practice-level characteristics that influence the impact of implementation strategies guided by practice facilitation in each clinical practice, to test whether the facilitator-driven provider- and practice-level implementation strategies increase provider recommendations and Human Papilloma Virus (HPV) vaccination rates and to evaluate implementation and future sustainability of the facilitator-driven implementation strategies across nine clinical practice sites
Condition
- Human Papillomavirus Infection
Eligibility
- Eligible Ages
- Between 11 Years and 17 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- FQHC's with less than 60% HPV vaccine initiation rate for 11-12 year old adolescents overall at their practice sites - FQHC's that have family medicine and/or pediatric practices - a total adolescent patient population at least 50% Latino - be willing for Health Care Provider (HCP) and staff members to receive education, training, and support; complete standardized measurement, and agree to randomization. - Providers, aged 18 and over, employed at each FQHC (4 staff per practice) - Staff, aged 18 and over, employed at each FQHC (5 staff per practice) - Implementation team members (i.e., administrative designee, health care providers, immunization navigators, and other staff), aged 18 and over, employed at each FQHC (4 members per practice) - Parents (aged 18 and over) of patients ages 11-17 seeking care at each FQHC (25 per practice).
Exclusion Criteria
- FQHCs that participated in the pilot study were excluded.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover Assignment
- Intervention Model Description
- This is a stepwise cluster randomized control design study. There will be 3 clusters (FQHC's) having 3 practices each
- Primary Purpose
- Prevention
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
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Experimental Step 1 (3 clinics)-15 months control then 30 months intervention |
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Experimental Step 2 (3 clinics)-21 months control then 24 months intervention |
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Experimental Step 3 (3 clinics)-27 months control then 18 months intervention |
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Recruiting Locations
The University of Texas Health Science Center at Houston
Houston, Texas 77030
Houston, Texas 77030
More Details
- Status
- Recruiting
- Sponsor
- The University of Texas Health Science Center, Houston