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Recruiting NCT06729775

Disentangling the Role of Culture, Life Stage, and Information Design to Facilitate Equity in Data Report Back

No phase Interventional Education, Health

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Data report back preference by life span.
Who it may be relevant to
Registry conditions: Education, Health. Basic parameters: from 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

There remains a need for novel research that facilitates RBRR in a manner that raises data and environmental health literacy (D/EHL) and supports communities striving for environmental health and structural change. Rooted in bioethics and building upon trusted and established long-term partnerships and leveraging existing datasets, the project goal is to create and pilot a national model of report back that is centered in the margins and engages diverse rural and urban EJ communities to ensure that RBRR reaches all populations in a manner tailored to their individual needs, including culture, life stage, language, and design.

Detailed description

The goal of this intervention study is to learn if the data report back design type can modify data and environmental health literacy learning outcomes in adolescence (10\~19 yrs.), young adults (18-26 yrs.) (110), and adults (27 yrs.+).

The main questions it aims to answer are:

* How does design type: (1) graphical (control), art-infused (treatment 1) and geospatial (treatment 2) influence data and environmental health literacy learning outcomes related to numeracy and data literacy? * How does design type: (1) graphical (control), art-infused (treatment 1) and geospatial (treatment 2) influence data and environmental health literacy learning outcomes related to knowledge and awareness related to environmental risks? * How does design type: (1) graphical (control), art-infused (treatment 1) and geospatial (treatment 2) influence data and environmental health literacy learning outcomes related to skills and self-efficacy for environmental action? * How does design type: (1) graphical (control), art-infused (treatment 1) and geospatial (treatment 2) influence data and environmental health literacy learning outcomes related to engaging in environmental health activities? * \[primary hypothesis or outcome measure 1\]? * \[primary hypothesis or outcome measure 2\]?

Researchers will compare outcomes related to life span and design type to see if the design type leads to difference data and environmental health literacy learning outcomes by life stage. During analysis, in addition to life stage, participants will also be analyzed by select sociodemographic variables, e.g., income, education, and race/ethnicity.

Participants will be asked to:

* Complete a pre-survey (baseline) * Complete a post-survey * Review their randomly assigned repot back design * Participate in a focus group and answer questions about the design * At minimum of six months later, participate in an interview

Summary statistics and qualitative summaries of findings will be generated and used to inform interpretation of inferential statistical tests comparing subgroups. Statistical analyses (i.e., Chi square tests, plus Cramér's V, Multivariate analysis of variance (MANOVA), Kruskal-Wallis, and/or Mann-Whitney U tests) will be conducted to determine any significant differences related to (1) numeracy and data literacy, (2) knowledge and awareness related to environmental risks and (3) skills and self-efficacy for environmental action occur by data report back design type and sociodemographic variables.

Interventions

  • Other Data report back preference by life span
    Data report back preference by life span.

Primary outcome measures

  • Changes from baseline in the mean literacy and numeracy based on questionnaire responses. [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Changes from baseline in the mean knowledge and awareness risks based on questionnaire responses. [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Changes from baseline in the mean skills and self-efficacy based on questionnaire responses. [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Changes from baseline in the mean environmental health engagement based on questionnaire responses. [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Number of participants reporting themes related to literacy and numeracy. [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Number of participants reporting themes related to knowledge and awareness risks [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Number of participants reporting themes related to skills and self-efficacy [Time frame: From enrollment to the end of treatment at 78 weeks]
  • Number of participants reporting themes related to environmental health engagement. [Time frame: From enrollment to the end of treatment at 78 weeks]

Eligibility criteria

Inclusion criteria

  • Participants should live in Pinal county, Arizona, Gila county, Arizona, and Cuyahoga county, Ohio.

Exclusion criteria

  • Individuals living outside of the partnering counties will not be eligible for participation.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • University of Arizona — Tucson

Identifiers

NCT: NCT06729775 · STUDY00004829 · R01ES036236

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗