Planetary Health and Environmental Justice in Construction Career Education (EJT-CTE)

January 2, 2026 updated by: Devan Cantrell Addison-Turner, Stanford University

Integrating Planetary Health and Environmental Justice Into High School Construction Career Education: A Randomized Controlled Trial of the Ecosystem Justice Translator

This study tests whether a new educational curriculum can help high school students in construction career programs better understand how building design affects community health and environmental justice. The study compares two approaches: (1) a new "Community-Centered Design" curriculum that uses the Ecosystem Justice Translator (EJT) software tool, which helps students see connections between construction decisions, energy efficiency, nature exposure, and health outcomes in different neighborhoods; versus (2) the traditional construction career curriculum that focuses on technical skills. Students aged 14-18 enrolled in construction career programs will be randomly assigned to one of these two groups. Over 6 months, the intervention group will learn to use the EJT tool and apply environmental justice concepts to construction projects. Researchers will measure how well students understand connections between construction, environment, and health at the start, middle, and end of the program, and again 6 months later. The goal is to determine if integrating environmental justice and health concepts into construction education improves students' awareness of how their future work can help or harm community health, particularly in disadvantaged neighborhoods.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Not yet recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Estimated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
40

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age 14-18 years at enrollment
  • Current enrollment in a participating construction career pathway program (minimum 2nd semester)
  • Ability to participate in 6-month curriculum during regular CTE class periods
  • Written informed consent from parent/guardian for participants under 18 years
  • Written assent from student participant
  • Ability to complete assessments in English (with accommodations as needed)

Exclusion Criteria:

  • Prior participation in a formal environmental justice or planetary health curriculum within the past 12 months
  • Expected inability to complete study assessments due to planned relocation or program withdrawal
  • Concurrent enrollment in another research study involving educational interventions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: Community-Centered Design Curriculum with EJT
6-month Community-Centered Design curriculum integrating the Ecosystem Justice Translator (EJT). Structure: Weeks 1-4 foundations of planetary health and environmental justice; Weeks 5-10 EJT module training; Weeks 11-18 community engagement project with local stakeholder interviews; Weeks 19-24 capstone design project. Delivered during regular CTE class periods (~4 hours weekly). Students work in teams of 3-4 on authentic community challenges. EJT is a web-based computational system with four modules: Community Voice Equity Translation (CVET), Ecosystem Service Health Integration (ESHI), Environmental Justice Investment Prioritization (EJIP), and Uncertainty, Bias, and Risk Quantification (UBR).
Behavioral: Community-Centered Design Curriculum with EJT
6-month (24-week) Community-Centered Design curriculum integrating the Ecosystem Justice Translator (EJT), delivered during regular CTE class periods (~4 hours weekly). EJT is a web-based computational system with four modules: (1) Community Voice Equity Translation using large language models; (2) Ecosystem Service Health Integration linking InVEST models with epidemiological dose-response functions; (3) Environmental Justice Investment Prioritization; (4) Uncertainty, Bias, and Risk Quantification. Curriculum structure: Weeks 1-4 planetary health foundations; Weeks 5-10 EJT training; Weeks 11-18 community engagement projects; Weeks 19-24 capstone design. Students work in teams of 3-4 on authentic community challenges.
Other Names:
  • Community-Centered Design Curriculum with Ecosystem Justice Translator
  • EJT Curriculum
Active Comparator: CONTROL
Standard construction career curriculum per California CTE Model Curriculum Standards: building codes and permitting, construction safety (OSHA 10), blueprint reading and computer-aided design (CAD), materials science and selection, basic carpentry and framing. Control participants receive equal contact hours (~4 hours weekly for 24 weeks) without explicit health equity, environmental justice, or planetary health content. Control participants will be offered access to intervention materials and EJT software after study completion (waitlist control design).
Behavioral: Traditional Technical Curriculum
Standard construction career curriculum per California CTE Model Curriculum Standards delivered over 24 weeks (~4 hours weekly). Content includes: building codes and permitting, construction safety (OSHA 10 certification), blueprint reading and CAD, materials science and selection, basic carpentry and framing techniques. Equal contact hours to intervention arm without explicit health equity, environmental justice, or planetary health content. Control participants offered access to EJT curriculum materials after study completion (waitlist control design).

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Health-Integrated Equity Consciousness Index (HI-ECI)
Time Frame: Baseline, 3 months, 6 months (primary endpoint), 12 months
Composite measure of awareness of relationships between built environment, energy systems, nature exposure, and health equity. Derived from coded qualitative responses to standardized scenario prompts. Higher scores indicate greater health equity consciousness. Range 0-100.
Baseline, 3 months, 6 months (primary endpoint), 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Stanford University

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Principal Investigator: Devan C. Addison-Turner, PhD in CEE, daddisonturner@stanford.edu

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
August 5, 2026

Primary Completion (Estimated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
May 30, 2027

Study Completion (Estimated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 12, 2027

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
December 20, 2025

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
December 20, 2025

First Posted (Estimated)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
January 5, 2026

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
January 7, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
January 2, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
January 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • IRB-84369
  • DGE-2146755 (Other Grant/Funding Number: National Science Foundation)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

I may keep anonymous, unique Individual Participant Data (IPD) for participant performance tracking in a codebook and database. The information may be used to publish a journal paper.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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