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Randomized Controlled Trial Testing a Training Program About Section 504 of the Rehabilitation Act

Understanding and Improving Access to Section 504 Among Students With Disabilities

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07710300
Enrollment
160
Registered
2026-07-17
Start date
2026-07-01
Completion date
2028-09-01
Last updated
2026-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Students With Disabilities and/or Family Members With Students With Disabilities That Have a Section 504 Plan

Keywords

Disability, Section 504, Section 504 plans

Brief summary

The goal of this training program is to learn if the intervention (i.e., training program) can improve access to Section 504 among students with disabilities and family caregivers. If students with disabilities and/or family caregivers are educated and empowered about Section 504, then there may be improved access to higher-quality of Section 504 plans. We aim to answer the following question: Is the training program effective? If there is a comparison group: We (our research team) will compare the intervention group to a waitlist-control group to discern differences in advocacy, empowerment, and knowledge and, subsequently, higher quality Section 504 plans and greater access to services. Participants will: * Attend an online class for an hour and a half each week for 6 weeks * Complete a pre-survey * Complete a formative evaluation after each program session * Complete a summative evaluation after the entire advocacy program * Complete a post-survey after completing the advocacy program * Complete a follow-up survey * Submit a copy of their child's (or their) Section 504 plan after providing consent

Interventions

OTHERTreatment

Training program about Section 504 for individuals with disabilities and/or family caregivers of an individual with disabilities.

OTHERMaterials-only control condition

Materials-only then access to advocacy training around Section 504 plans for individuals with disabilities and/or family caregivers of individuals with disabilities. Will have advocacy training 6 months after the control group.

Sponsors

Vanderbilt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

This is a randomized controlled trial with a waitlist-control group.

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

The participant must be willing to complete the research measures and the training program as well as meet one of the two following criteria: * be a student aged 12-21 who receives Section 504 supports during K-12 school * be the caregiver of a child who receives Section 504 supports during K-12 school

Design outcomes

Primary

MeasureTime frameDescription
Knowledge of Section 504From enrollment to the end of the training program at six weeksThis is a 20 item measure; each item has four response options. Only one response option is correct. The score is the sum of correct responses ranging from 0 to 20.
Advocacy Activities ScaleFrom enrollment to the end of the training program at six weeksThis is a 15 item measure wherein each item has four response options. The final score is the sum of the response options.
EmpowermentFrom enrollment to the end of the training program at six weeksThis is a 34 item measure wherein each item has four responses. The score is the sum of the responses.

Secondary

MeasureTime frameDescription
Quality of the Section 504 planFrom enrollment to six months after the end of the training programThis is a rubric which gauges the quality of the Section 504 plan. The score reflects a range from 0-15 of needed items on the Section 504 plan.
Service accessFrom enrollment to six months after the end of the training programThis is a 24 item measure that examines whether a certain support is received. The score is the sum of received supports (ranging from 0-24).

Countries

United States

Contacts

CONTACTMeghan M Burke, Dr.
meghan.burke@vanderbilt.edu615-343-1014

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026