Overview
Title
Agency Information Collection Activities; Survey of Young Adults on the Autism Spectrum for the Research Support Services for Employment of Young Adults on the Autism Spectrum (REYAAS) Project
Agencies
ELI5 AI
The Department of Labor wants to ask young people with autism about their work experiences to help make better rules and programs for them. They want to know what people think about this idea and will listen to comments until April 23, 2025.
Summary AI
The Department of Labor (DOL) is asking for public comments on a new survey they want to conduct about young adults on the autism spectrum. This survey, part of the Research Support Services for Employment of Young Adults on the Autism Spectrum (REYAAS) Project, aims to gather data on the experiences of autistic young adults in the workforce to help improve policies and programs. The public can write comments about the necessity and impact of this information collection by April 23, 2025. More details can be obtained by contacting Nicole Bouchet at the DOL.
Abstract
The Department of Labor (DOL) is submitting this Office of Disability Employment Policy (ODEP)-sponsored information collection request (ICR) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995 (PRA). Public comments on the ICR are invited.
Keywords AI
Sources
AnalysisAI
The Federal Register document in question is a notice from the Department of Labor (DOL) inviting public comments on a proposed information collection initiative. The initiative, part of the Research Support Services for Employment of Young Adults on the Autism Spectrum (REYAAS) Project, seeks to conduct a survey of young adults on the autism spectrum to gather data on their employment experiences. The goal is to use this information to inform and potentially improve policies and programs that support the employment of autistic individuals.
General Summary
The DOL has reached out for public input on a planned survey targeting autistic young adults aged 16 to 28. This initiative, managed under the Office of Disability Employment Policy (ODEP), aims to explore the challenges and opportunities faced by this demographic in the workplace. The survey will gather both quantitative data through the survey itself and qualitative insights from follow-up interviews. Interested parties are encouraged to provide feedback by April 23, 2025, on the perceived necessity, potential utility, and the methodological approach of this data collection.
Significant Issues and Concerns
One notable concern is the absence of a detailed explanation of how the gathered information will tangibly enhance employment outcomes for autistic young adults. While the survey's intent is clear, without a mapped-out strategy for applying the results, its practical impact remains uncertain.
Additionally, while the document outlines the estimated burden in terms of hours, it lacks transparency on how this time commitment will be spread across activities or respondents. No other costs are mentioned, which might omit potential indirect costs that could arise, such as technological or logistical requirements for participation.
The language used includes terms that might be challenging for some readers, such as "practical utility" and "methodology and assumptions used," without offering simpler explanations or context, potentially limiting understanding for those unfamiliar with the nuances of policy research.
Moreover, the document does not specify how survey findings will be utilized to advocate for policy or programmatic changes. This lack of specificity may cause apprehension among stakeholders eager to see concrete, actionable results.
Impact on the Public
Broadly, this document could signal a positive step toward understanding and addressing the employment challenges faced by young autistic adults. By encouraging public comment, the DOL seems committed to making the process inclusive and reflective of community needs and insights.
However, the potential positive impact might be dampened if the public perceives the survey as a nominal effort rather than a conduit for significant policy improvement. Effective dissemination of the survey findings and their applications will be crucial to gaining public trust.
Impact on Specific Stakeholders
For autistic young adults, the project holds the promise of contributing toward making workplaces more inclusive and understanding of their needs. Yet, this potential impact hinges on clear communication about how the data will be turned into actionable changes.
For policymakers and advocacy groups within the autism community, the survey could furnish valuable data to support their efforts in crafting supportive environments. However, the current lack of detailed follow-through plans might obscure strategic engagement and actionable policy proposals.
In conclusion, while the survey has the potential to serve as a foundation for meaningful change, its success is likely to depend on transparency, inclusivity, and the practical application of its findings to influence policy and program development.
Financial Assessment
The document contains a reference to the estimated financial implications of the information collection activity conducted by the Department of Labor’s Office of Disability Employment Policy. Specifically, it mentions a Total Estimated Annual Other Costs Burden of $0. This essentially means that, beyond the time investment required from respondents, there are no anticipated monetary costs incurred by those participating in this data collection effort.
However, this reference to a $0 cost may raise questions among stakeholders. One of the identified issues in the document pertains to the potential for indirect costs that might not have been accounted for within the survey. While the document asserts that no additional financial burden will be imposed on the participants, some indirect expenses, such as potential costs related to internet usage or resources used during extended survey interactions, are not detailed. Although these are typically minor, they could still be perceived as costs by some participants. Therefore, an explicit acknowledgment or clarification of these possible indirect costs could help mitigate any concerns of stakeholders regarding hidden financial implications.
Additionally, while the Total Estimated Annual Time Burden is specified as 1,265 hours, the financial aspects mentioned do not cover potential opportunity costs. Time spent by respondents, which might otherwise be utilized at a monetary advantage—like paid work—is a crucial factor. Acknowledging this dimension could offer a more comprehensive view of the 'cost' implications, even if individuals are not directly paying out-of-pocket expenses to participate in the data collection process. By addressing these elements, the Department could provide clarity and reinforce transparency in its communication, aligning with the objective of soliciting public comments effectively.
Overall, the financial references in the document emphasize an absence of direct costs, but a more nuanced explanation of indirect costs and opportunity costs could be beneficial for a more informed public discourse.
Issues
• The document provides a clear outline of the request for comments but does not specify how the information collected will directly improve employment outcomes for autistic young adults, which could lead to questions about the practical utility of the survey.
• The total estimated annual time burden and number of respondents are provided, but there is no breakdown of what this time burden entails, which could lead to ambiguity regarding the commitment required from respondents.
• There is no cost burden mentioned apart from time, which could be misleading if there are indirect costs to respondents not accounted for.
• The language is generally clear, but terms like 'practical utility' and 'methodology and assumptions used' are not explained, which might be overly complex for individuals unfamiliar with the subject matter.
• The document does not explain how the survey results will be used to influence policy or program changes, which might be a concern for stakeholders interested in the tangible outcomes of this research.
• While the survey is designed to benefit young adults on the autism spectrum, the document lacks specific details on how the results will be shared with or utilized by the autism community, leading to a potential gap in stakeholder communication.