Beyond Functional Limits: Unpacking the Clinical Diagnoses Behind Federal Disability Surveys

Beyond Functional Limits: Unpacking the Clinical Diagnoses Behind Federal Disability Surveys

Introduction: The Functional Framework of Disability Data

The American Community Survey 6-Question Sequence (ACS-6) serves as the primary tool for federal data collection on disability in the United States. Designed to capture functional limitations rather than specific clinical diagnoses, the ACS-6 asks respondents about difficulties with hearing, vision, cognition, mobility, self-care, and independent living. These data points are critical; they influence the allocation of billions of dollars in federal funding, guide civil rights enforcement, and shape public health policy. However, a significant gap has persisted in our understanding: what specific clinical conditions are actually represented within these functional categories?

The Clinical Importance of Characterizing Disability

For clinicians and health policy experts, the distinction between functional impairment and medical diagnosis is vital. While the social model of disability emphasizes environmental barriers and functional outcomes, the medical model provides the necessary specificity for targeted interventions, resource planning, and understanding the disease burden within the disabled population. A new study published in JAMA Health Forum by Ari Ne’eman investigates this intersection, providing a detailed characterization of the diagnoses reported by individuals identified as disabled by the ACS-6 sequence.

Study Design and Methodology

This cross-sectional study utilized data from the 2023 or 2024 Survey of Income and Program Participation (SIPP), a nationally representative survey that includes both the ACS-6 questions and more granular questions regarding specific medical diagnoses. The researcher analyzed a sample of 13,341 individuals who identified as having a disability according to the ACS-6 criteria. The primary objective was to assess the prevalence of 36 different diagnosis groupings and determine if these patterns varied across demographic lines, including age, race, ethnicity, sex, and educational attainment. The data analysis was conducted between August and September 2025.

Key Findings: The Prevalence of Mental Health and Musculoskeletal Conditions

The study’s results reveal a complex landscape of disability in the United States, particularly among the working-age population (ages 22 to 64). Contrary to traditional stereotypes of disability being primarily characterized by visible physical or sensory impairments, the most frequent diagnoses reported were mental health and non-specific physical ailments.

Working-Age Population (22–64 Years)

Among respondents in this age bracket, the five most common diagnosis groupings were: 1. Anxiety or Obsessive-Compulsive Disorders (15.6%; 95% CI, 14.5%-16.9%) 2. Depression (15.3%; 95% CI, 14.1%-16.5%) 3. Unspecified Musculoskeletal Issues (13.5%; 95% CI, 12.5%-14.6%) 4. Back or Spinal Problems (11.6%; 95% CI, 10.6%-12.6%) 5. Unspecified Neurologic Disorders (10.8%; 95% CI, 9.8%-11.8%) These findings underscore the high burden of psychiatric and musculoskeletal morbidity within the disabled community, suggesting that functional limitations in cognition or mobility are often rooted in these prevalent conditions.

Demographic Consistency vs. Age-Related Heterogeneity

One of the study’s most significant findings is that the ACS-6 identifies a clinically similar population across most demographic subgroups. When disaggregated by sex, race, ethnicity, and educational level, the most common diagnoses remained relatively consistent. This suggests that the ACS-6 is a robust tool for identifying a specific type of functionally limited population regardless of socioeconomic or cultural background. However, age proved to be a major differentiator. The diagnostic profile of a 25-year-old identified as disabled via the ACS-6 is vastly different from that of a 75-year-old. While mental health conditions dominate the younger cohorts, age-related degenerative conditions, sensory loss, and chronic systemic diseases become more prevalent in older populations. This heterogeneity highlights that ‘disability’ as captured by federal surveys is not a monolithic experience.

Clinical and Policy Implications

The findings have profound implications for how healthcare providers and policymakers approach disability.

The Mental Health Crisis in Disability Policy

The high prevalence of anxiety and depression among those identified as disabled by the ACS-6—particularly those who report cognitive disabilities—indicates that federal disability metrics are capturing a significant portion of the population struggling with severe mental health challenges. This suggests that policies aimed at supporting the disabled must integrate robust psychiatric and behavioral health components.

Addressing the Musculoskeletal Burden

The prominence of back, spinal, and unspecified musculoskeletal issues highlights the ongoing need for improved pain management, physical therapy, and ergonomic interventions. It also points to the potential impact of occupational hazards on long-term disability status.

Survey Revision and Granularity

There is an ongoing debate regarding the future of federal disability data collection. Some advocates and researchers have called for more granular questions that could better differentiate between types of disabilities. Ne’eman’s study suggests that while the ACS-6 is effective at identifying a consistent population across many demographics, it may obscure the significant clinical diversity within that population. Future survey designs may need to balance the simplicity of functional questions with the depth of diagnostic data to better serve public health needs.

Study Limitations

It is important to note that the diagnoses were self-reported by survey respondents. While self-reporting is a standard method in large-scale population surveys, it may be subject to recall bias or a lack of clinical precision compared to electronic health record (EHR) data. Additionally, the study’s cross-sectional nature means it can identify associations but cannot establish temporal or causal relationships between a diagnosis and the onset of functional impairment.

Conclusion: A Call for Targeted Support

The ACS-6 remains a vital tool for identifying people with disabilities in the U.S., but as this research demonstrates, the population it identifies is clinically diverse. The dominance of mental health and musculoskeletal conditions among working-age adults challenges traditional perceptions of disability and calls for a more nuanced approach to healthcare delivery and social support systems. As federal agencies consider revisions to how they measure disability, they must account for this clinical heterogeneity to ensure that the needs of all disabled individuals are met with precision and equity.

References

Ne’eman A. Disability Diagnoses Identified by the American Community Survey 6-Question Sequence. JAMA Health Forum. 2026;7(1):e256302. doi:10.1001/jamahealthforum.2025.6302.

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