Abstract
Background: Colorectal cancer (CRC) screening is crucial for early detection, but people with intellectual and
developmental disabilities (IDD) face significant healthcare disparities, including lower screening rates.
Objective: This study explores barriers and facilitators to CRC screening for individuals with IDD from the
caregiver perspective.
Methods: Semi-structured interviews were conducted with 13 caregivers (eight women, mean age 45) of in-
dividuals with IDD in Austria and analyzed using thematic analysis. A modified version of the Bowel Cancer
Awareness Measure (CAM) questionnaire was used to assess CRC-related healthcare literacy of the caregivers.
Results: The modified CAM revealed low CRC knowledge among caregivers, with gaps in symptom and risk factor
recognition and low self-reported confidence in symptom detection. Four themes emerged from the interviews:
(1) Improving access to inclusive healthcare, highlighting systemic healthcare challenges, inclusive environments,
clinician expertise, and health education; (2) Managing IDD-specific challenges, including communication diffi-
culties, reliance on routines, and comorbidities; (3) The critical role of caregiver support, focusing on the
empowerment of people with IDD; and (4) Challenging stigma and bridging social gaps, addressing stereotypes and
social segregation of people with IDD.
Conclusions: This study serves as a case study, illustrating how the exclusion of people with IDD from the design
of preventive healthcare perpetuates inequities in CRC screening, and emphasizing the need for more inclusive
systems and practices. Addressing these shortcomings requires improved knowledge and educational resources,
disability-sensitive training for professionals, accessible healthcare environments and systemic efforts to promote
autonomy and reduce stigma.
developmental disabilities (IDD) face significant healthcare disparities, including lower screening rates.
Objective: This study explores barriers and facilitators to CRC screening for individuals with IDD from the
caregiver perspective.
Methods: Semi-structured interviews were conducted with 13 caregivers (eight women, mean age 45) of in-
dividuals with IDD in Austria and analyzed using thematic analysis. A modified version of the Bowel Cancer
Awareness Measure (CAM) questionnaire was used to assess CRC-related healthcare literacy of the caregivers.
Results: The modified CAM revealed low CRC knowledge among caregivers, with gaps in symptom and risk factor
recognition and low self-reported confidence in symptom detection. Four themes emerged from the interviews:
(1) Improving access to inclusive healthcare, highlighting systemic healthcare challenges, inclusive environments,
clinician expertise, and health education; (2) Managing IDD-specific challenges, including communication diffi-
culties, reliance on routines, and comorbidities; (3) The critical role of caregiver support, focusing on the
empowerment of people with IDD; and (4) Challenging stigma and bridging social gaps, addressing stereotypes and
social segregation of people with IDD.
Conclusions: This study serves as a case study, illustrating how the exclusion of people with IDD from the design
of preventive healthcare perpetuates inequities in CRC screening, and emphasizing the need for more inclusive
systems and practices. Addressing these shortcomings requires improved knowledge and educational resources,
disability-sensitive training for professionals, accessible healthcare environments and systemic efforts to promote
autonomy and reduce stigma.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 101967 |
| Fachzeitschrift | Disability and Health Journal |
| Jahrgang | 19 |
| Frühes Online-Datum | 16 Sept. 2025 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - Jan. 2026 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
-
SDG 3 – Gesundheit und Wohlergehen
ÖFOS 2012
- 303026 Public Health
- 501010 Klinische Psychologie
- 302055 Onkologie
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