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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03820011
Other study ID # 2016-0600
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2016
Est. completion date August 1, 2020

Study information

Verified date April 2024
Source University of Illinois at Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of the proposed research is to achieve a major advance in promoting effective and efficient delivery of pediatric rehabilitation services for young children with developmental disabilities and delays. The investigative team will examine the usability, feasibility, acceptability, and preliminary effects of PEM+, an innovative web-based (mobile friendly) guide for care planning by parents of young children with developmental disabilities and delays. PEM+ is designed in partnership with parents and providers to support more collaborative and efficient clinical care planning with individual families who typically access pediatric occupational therapy services. Specifically, PEM+ enables parents to build on their baseline assessment of their child using the Young Children's Participation and Environment Measure (YC-PEM) to design specific solutions to their young child's participation-related problems. PEM+ affords parents the opportunity to do this in their own space and on their own schedule, as well as electronically share their proposed written solutions with their child's provider(s) and/or other important individuals in their young child's life.


Description:

Participation and Environment Measure Plus (PEM+) is a new electronic health application that facilitates family-centered and participation-focused intervention planning for young children receiving rehabilitation therapies. PEM+ design was informed by caregiver and provider input. It is a web-based intervention planning application that is designed for use by caregivers of young children receiving rehabilitation therapies. Caregivers who complete the Young Children's Participation and Environment Measure (YC-PEM), an electronic patient-reported outcome measure, evaluate their child's participation and then can click on a weblink to begin the PEM+ application, whereby they build on their YC-PEM responses for the purpose of creating a participation-focused care plan to share with their child's rehabilitation team. PEM+ is a five-step recursive process (i.e., the caregiver can repeat the five-step process to create as many care plans for their child as needed), and it offers tiered support to the user during completion (tier 1: frequently asked questions available in the application, tier 2: support provided by email, tier 3: support provided by phone). For the first aim of this study, caregivers completed one iteration of PEM+ to complete user tasks for the purpose of evaluating PEM+ usability. For the second aim of this study, caregivers were instructed to complete the PEM+ over a two-week (14 day) period. This time frame was selected by the research team as it mimics what would be provided in the routine care planning processes of early intervention and early childhood education.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date August 1, 2020
Est. primary completion date February 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Aim 1 Inclusion Criteria: - at least 18 years old - reads, writes, and speaks English - has access to broadband internet - resides in the U.S - has a child between 0 and 3 years old who is receiving services for developmental delay. Aim 1 Exclusion Criteria: - has a child over 3 years old - does not have internet access - has a child who is not receiving rehabilitation services for developmental delay - does not reside in the U.S. Aim 2 Inclusion Criteria: - 18 years or older - reads, writes, and speaks in English - has a child aged 0-5 years old who was receiving rehabilitation services - has broadband internet access - denotes at least one area of desired change during participation assessment. Aim 2 Exclusion Criteria: - has a child over 5 years old - does not have internet access - has a child who is not receiving rehabilitation services for developmental delay - does not reside in the U.S.

Study Design


Intervention

Other:
PEM+
PEM+ is a five-step recursive process (i.e., the caregiver can repeat the five-step process to create as many intervention plans for their child as needed, relative to the number of activities in which change is desired based on the YC-PEM e-PRO, and it offers tiered support to the user during completion (tier 1: frequently asked questions available in the application, tier 2: support provided by email, tier 3: support provided by phone).

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Mary A Khetani McGill University, McMaster University

Outcome

Type Measure Description Time frame Safety issue
Primary Mean Retention Rates As an indicator of PEM+ feasibility, we used web analytics to obtain estimates of the percentage of caregivers who enrolled completed the trial. Following completion of two-week trial
Primary Median PEM+ Completion Time As an indicator of PEM+ feasibility, we used web analytics to estimate the median time for completing the first and subsequent iterations within a two-week trial period Following completion of PEM+ iteration (Aim 1) and two weeks (Aim 2)
Primary Percentage of Caregivers Completing PEM+ Independently As an indicator of PEM+ feasibility, we used web analytics to estimate proportion of care plans created Following completion of two-week trial
Primary Median Number of PEM+ Care Plans Created As an indicator of PEM+ feasibility, we used web analytics estimate the number of care plans created over a two-week trial period. Following completion of two-week trial
Primary Usefulness, Satisfaction, and Ease of Use Questionnaire (USE) As an indicator of PEM+ acceptability, the USE is a questionnaire that evaluates usefulness, ease of use, ease of learning, and satisfaction. Items are on a 7-point scale, from from [1] strongly disagree, to [7] strongly agree. There were multiple items for each domain, which were summed together and divided by the total number of items to generate a summary score for that domain. Higher scores indicate a better outcome. Following completion of two-week trial
Primary Caregiver Self-Efficacy to Promote Child's Participation in Activities As an indicator of preliminary effects, we developed two items for this project to estimate caregiver self-efficacy in caring for their child, according to "what I will do next [to support child's participation]" and "how I think [about my child's participation]". Each item was rated on a 7-point scale, from [1] strongly disagree, to [7] strongly agree. Higher scores indicate a better outcome. Following completion of two-week trial
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