Electronic Patient-reported Outcomes (e-PROs) in Early Intervention

Developmental Disability Clinical Trial

Official title:

Colorado Early Intervention Outcomes Research Using Innovative Patient-Reported Outcome (PRO) Measures

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03904797
• Other study ID #: 2016-0139
• Status: Completed
• Phase: N/A
• Start date: April 1, 2016
• Est. completion date: February 1, 2019

Study information

• Verified date: March 2019
• Source: University of Illinois at Chicago
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A major goal of early intervention (EI) is to employ a family-centered approach to helping children to optimally function at home and in the community. However, the effects of EI are poorly understood. The aims of this project are: 1) to test the feasibility, acceptability, and value of introducing novel electronic patient-reported outcome (e-PRO) measures in EI, to strengthen family-centered EI care; and 2) to obtain and pair these outcomes data with EI program data, to further determine the value of e-PRO data collection for examining links between EI service use and functional outcomes among families who are enrolled in a large, urban EI program.

Description:

Approximately 5,800 infants and toddlers with developmental disabilities (e.g., cerebral palsy, Down syndrome, complex chronic conditions) and delays access Early Intervention Colorado (EI-CO) annually. A primary goal of EI-CO is to employ a family-centered care approach to help children optimally function at home and in the community. Hence, early intervention is a common source of rehabilitation (i.e., physical, occupational, speech and language therapy) for EI-CO eligible families.

However, the effects of EI-CO are poorly understood. Numerous challenges exist with obtaining EI-CO outcomes data, including a paucity of validated and feasible functional outcome measures for use in EI outcomes reporting. These challenges have resulted in inadequate knowledge about EI service use and outcomes to guide service delivery. Despite these challenges, recent policy changes have resulted in EI-CO service providers being pressed to ensure high quality care with limited resources and evidence to guide their clinical decision-making about effective and efficient interventions. This proposal addresses the need to fill critical knowledge gaps about the adequacy of EI services with an eye toward improving care quality.

This study involves families who have/are receiving EI-CO services through Rocky Mountain Human Services (RMHS), the largest EI program in Denver Metro. The purpose of this study is to test the feasibility, acceptability, and value of collecting electronic patient-reported outcomes (e-PRO) data to engage families when their child is due for an annual evaluation of progress. To further demonstrate the value of e-PRO data collection, these data will be paired with program data to estimate the association between EI-CO service use and functional outcomes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 149
• Est. completion date: February 1, 2019
• Est. primary completion date: September 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Month to 36 Months

Eligibility

Inclusion Criteria:

• Caregiver is at least 18 years old;

• Caregiver can read, write, and speak English or Spanish;

• Caregiver had internet access;

• Caregiver has a child between 0-3 years old who had received early intervention at RMHS for at least 3 months.

Exclusion Criteria:

• Caregiver is less than 18 years old

• Caregiver reads, speaks, and writes in a language other than English or Spanish

• Caregiver does not have internet access

• Caregiver has a child who has received EI services for less than 3 months

• Caregiver has a child older than 3 years (36 months)

Related Conditions & MeSH terms

• Development Delay
• Developmental Disabilities
• Developmental Disability

Intervention

Behavioral:
• Young Children's Participation and Environment Measure (YC-PEM) electronic patient-reported outcome (e-PRO)
Participants were primary caregivers (n=149) recruited from a large, urban early intervention program. All caregivers were approached by early intervention staff the month prior to the child's annual evaluation of progress. Each caregiver confirmed his or her eligibility online by verifying that they were at least 18 years old; could read, write, and speak English or Spanish; had internet access; and had a child between 0-3 years old who had received early intervention for at least 3 months. Participants enrolled online and provided consent, signed a HIPAA authorization for service record release, and then proceeded to completing a demographic questionnaire and YC-PEM e-PRO to receive an online report of their responses to share with their child's EI team.

Locations

Country	Name	City	State
n/a

Sponsors (3)

Lead Sponsor	Collaborator
University of Illinois at Chicago	Rocky Mountain Human Services, University of Colorado, Denver

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	YC-PEM e-PRO Feasibility as assessed by enrollment rate	Enrollment rate was estimated as the proportion of eligible participants who enrolled in the study. The success of feasibility was determined as e-PRO enrollment rates of 50% or higher based on what is known about the percentage of families who opt into family assessment as part of usual care.	up to 4 weeks
Primary	YC-PEM e-PRO Acceptability as assessed by caregiver perceptions of overall helpfulness	Caregiver responses to an open-ended item were coded into a one of three categories (yes, helpful; somewhat helpful; not helpful) to create a new variable that captured the extent to which caregivers perceived the YC-PEM e-PRO to be useful for planning EI care.	up to 4 weeks
Primary	YC-PEM e-PRO Value as assessed by proportion of participants viewing e-PRO online report	The percentage of participants who viewed a summary of their e-PRO responses via an online report was estimated.	up to 4 weeks
Primary	YC-PEM e-PRO Feasibility as assessed by completion rate	Feasibility was determined as the proportion of participants who enrolled that completed the YC-PEM e-PRO. The success of feasibility was determined as completion rates of 50% or higher based on family assessment completion rates within usual care.	up to 4 weeks
Primary	YC-PEM e-PRO Feasibility as assessed by completion time in minutes and seconds	The success of feasibility was determined as e-PRO completion time of less than 45 minutes based on family assessment completion time within usual care.	up to 4 weeks