Participant Experience Survey Mental Retardation/Developmental Disabilities Version (PES-MRDD)

Overview

Purpose
State quality assurance
Respondents
  • Proxy
  • Person with a Disability
Administration Method
Interview
Administration Mode
In-person
Developer
MEDSTAT
Item Count
83
Population
Intellectual and Developmental Disability
Coverage Area
Unclear if these are the same coverage area for each survey

Instrument Citation(s)

The MEDSTAT Group, Inc. (2003). Participant Experience Survey MR/DD Version. http://nasuad.org/hcbs/article/participant-experience-survey-pes-tools

The MEDSTAT Group, Inc. (2003). Participant Experience Survey MR/DD Version Users’ Guide. http://nasuad.org/hcbs/article/participant-experience-survey-pes-tools

Instrument Domains

DomainNumber of Items
Choice and Control21
Choice of services and supports2
Personal choices and goals11
Personal freedoms and dignity of risk8
Self-direction3
Community Inclusion13
Employment3
Meaningful activity8
Social connectedness and relationships3
Transportation1
Resources and settings to facilitate inclusion0
Holistic Health and Functioning2
Individual health and functioning2
Health promotion and prevention0
Human and Legal Rights9
Freedom from abuse and neglect3
Informed decision-making1
Optimizing the preservation of legal and human rights3
Privacy3
Supporting individuals in exercising their human and legal rights0
Person-Centered Planning and Coordination13
Assessment13
Coordination0
Person-centered planning0
Service Delivery and Effectiveness15
Delivery14
Person's needs met and goals realized13
Workforce22
Demonstrated competencies when appropriate1
Person-centered approach to services10
Sufficient workforce numbers dispersion and availability11
Adequately compensated with benefits0
Culturally competent0
Safety of and respect for the worker0
Staff Turnover0
Workforce engagement and participation0
Caregiver Support0
Access to resources0
Family caregiver/natural support involvement0
Family caregiver/natural support wellbeing0
Training and skill-building0
Consumer Leadership in System Development0
Evidence of meaningful caregiver involvement0
Evidence of meaningful consumer involvement0
System supports meaningful consumer involvement0
Equity0
Availability0
Equitable access and resource allocation0
Transparency and consistency0
Fluctuation of Need0
Level of Caregiver Well-Being0
System Performance and Accountability0
Data management and use0
Evidence-based practice0
Financing and service delivery structures0