Louisa A Stark
Biographic Data
| ID | 3573011 |
|---|---|
| NAME | Louisa A Stark |
| GIVEN NAMES | Louisa A |
| FAMILY NAME | Stark |
| SIGNATURE | STARK L A |
| AFFILIATIONS | University of Utah |
| ORCID | 0000-0002-2978-7279 |
| VERIFIED | Yes |
| TOTAL WORKS | 12 |
| TOTAL CITATIONS | 6 |
| WORKS AS AUTHOR | 12 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 1988 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 2 |
Prenatal Education to Support Pregnant People's Awareness, Knowledge, and Reported Oral Exposure and Risk Reduction Behaviors Surrounding Congenital Cytomegalovirus
Simple educational materials can improve knowledge of cCMV during pregnancy, but more intensive intervention may be needed to change behaviors, especially for individuals who experience barriers to implementing risk reduction behaviors
Electronic informed consent information for residual newborn specimen research
Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research
Obtaining informed consent for bloodspot research from newborn screening is particularly challenging due to the hectic environment of the postnatal period and the relatively abstract nature of future, unspecified research on the biospecimens. A randomized controlled trial was conducted in three Michigan hospitals to compare two different consent processes (video and interactive tablet "app") with standard brochure-based consent in the Michigan Bi…
Factors Associated with Human Papillomavirus Vaccination Among Diverse Adolescents in a Region with Low Human Papillomavirus Vaccination Rates
Introduction: This study assesses the sociodemographic facilitators and barriers to human papillomavirus (HPV) vaccination for diverse teens in a region with low HPV vaccination rates. Materials and Methods: In this community-based participatory research study, we surveyed adult family members of teens aged 11–17 years from African American, African refugee, American Indian/Alaskan Native, Hispanic/Latino, and Native Hawaiian/Pacific Islander com…
Diverse caregivers’ HPV vaccine-related awareness and knowledge
Objectives: To assess factors associated with HPV vaccine-related awareness and knowledge among caregivers of adolescents from five ethnic community groups in Utah. Design: For this community-based participatory research study, we surveyed N = 228 caregivers of teens aged 11-17 years from African American, African refugee, American Indian/Alaskan Native, Hispanic/Latino, and Native Hawaiian/Pacific Islander community groups in Utah about their HP…
Public attitudes regarding the use of electronic health information and residual clinical tissues for research
A Randomized Controlled Trial of an Electronic Informed Consent Process
A pilot study assessed an electronic informed consent model within a randomized controlled trial (RCT). Participants who were recruited for the parent RCT project were randomly selected and randomized to either an electronic consent group (n = 32) or a simplified paper-based consent group (n = 30). Results from the electronic consent group reported significantly higher understanding of the purpose of the study, alternatives to participation, and …
Public attitudes regarding the use of electronic health information and residual clinical tissues for research
Assessing public attitudes on the retention and use of residual newborn screening blood samples
Concerns of Newborn Blood Screening Advisory Committee Members Regarding Storage and Use of Residual Newborn Screening Blood Spots
Objectives. We assessed attitudes and opinions of members of newborn blood screening (NBS) advisory committees regarding the storage and secondary research use of residual specimens from NBS. Methods. We conducted focus groups in 2008 and 2009 with NBS advisory committees (4 focus groups; n = 39 participants) in the Mountain States region (i.e., AZ, CO, MT, NM, NV, TX, UT, and WY). Results. Participants identified several challenges to implementi…
Health care for the homeless
Supplementary Statement on Health Care for Homeless People
Assessing public attitudes on the retention and use of residual newborn screening blood samples
Supplementary Statement on Health Care for Homeless People
Diverse caregivers’ HPV vaccine-related awareness and knowledge
Objectives: To assess factors associated with HPV vaccine-related awareness and knowledge among caregivers of adolescents from five ethnic community groups in Utah. Design: For this community-based participatory research study, we surveyed N = 228 caregivers of teens aged 11-17 years from African American, African refugee, American Indian/Alaskan Native, Hispanic/Latino, and Native Hawaiian/Pacific Islander community groups in Utah about their HP…
A Randomized Controlled Trial of an Electronic Informed Consent Process
A pilot study assessed an electronic informed consent model within a randomized controlled trial (RCT). Participants who were recruited for the parent RCT project were randomly selected and randomized to either an electronic consent group (n = 32) or a simplified paper-based consent group (n = 30). Results from the electronic consent group reported significantly higher understanding of the purpose of the study, alternatives to participation, and …
Supplementary Statement on Health Care for Homeless People
Health care for the homeless
Concerns of Newborn Blood Screening Advisory Committee Members Regarding Storage and Use of Residual Newborn Screening Blood Spots
Objectives. We assessed attitudes and opinions of members of newborn blood screening (NBS) advisory committees regarding the storage and secondary research use of residual specimens from NBS. Methods. We conducted focus groups in 2008 and 2009 with NBS advisory committees (4 focus groups; n = 39 participants) in the Mountain States region (i.e., AZ, CO, MT, NM, NV, TX, UT, and WY). Results. Participants identified several challenges to implementi…
Assessing public attitudes on the retention and use of residual newborn screening blood samples
Public attitudes regarding the use of electronic health information and residual clinical tissues for research
A Randomized Controlled Trial of an Electronic Informed Consent Process
A pilot study assessed an electronic informed consent model within a randomized controlled trial (RCT). Participants who were recruited for the parent RCT project were randomly selected and randomized to either an electronic consent group (n = 32) or a simplified paper-based consent group (n = 30). Results from the electronic consent group reported significantly higher understanding of the purpose of the study, alternatives to participation, and …
Public attitudes regarding the use of electronic health information and residual clinical tissues for research
Factors Associated with Human Papillomavirus Vaccination Among Diverse Adolescents in a Region with Low Human Papillomavirus Vaccination Rates
Introduction: This study assesses the sociodemographic facilitators and barriers to human papillomavirus (HPV) vaccination for diverse teens in a region with low HPV vaccination rates. Materials and Methods: In this community-based participatory research study, we surveyed adult family members of teens aged 11–17 years from African American, African refugee, American Indian/Alaskan Native, Hispanic/Latino, and Native Hawaiian/Pacific Islander com…
Diverse caregivers’ HPV vaccine-related awareness and knowledge
Objectives: To assess factors associated with HPV vaccine-related awareness and knowledge among caregivers of adolescents from five ethnic community groups in Utah. Design: For this community-based participatory research study, we surveyed N = 228 caregivers of teens aged 11-17 years from African American, African refugee, American Indian/Alaskan Native, Hispanic/Latino, and Native Hawaiian/Pacific Islander community groups in Utah about their HP…
Comparison of Video, App, and Standard Consent Processes on Decision-Making for Biospecimen Research
Obtaining informed consent for bloodspot research from newborn screening is particularly challenging due to the hectic environment of the postnatal period and the relatively abstract nature of future, unspecified research on the biospecimens. A randomized controlled trial was conducted in three Michigan hospitals to compare two different consent processes (video and interactive tablet "app") with standard brochure-based consent in the Michigan Bi…
Electronic informed consent information for residual newborn specimen research
Prenatal Education to Support Pregnant People's Awareness, Knowledge, and Reported Oral Exposure and Risk Reduction Behaviors Surrounding Congenital Cytomegalovirus
Simple educational materials can improve knowledge of cCMV during pregnancy, but more intensive intervention may be needed to change behaviors, especially for individuals who experience barriers to implementing risk reduction behaviors
Medicine (11 works) · Ethics in Clinical Research (7 works) · Family medicine (6 works) · Alternative medicine (5 works) · Informed consent (5 works) · Medical education (5 works) · Political science (5 works) · Psychology (5 works) · Environmental health (4 works) · Focus group (4 works)