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Participation and Environment Measure-Plus (PEM-Plus) Care Planning Intervention (PEM-Plus)

Primary Purpose

Developmental Disability, Early Intervention (Education)

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
PEM+
Sponsored by
Mary A Khetani
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Developmental Disability focused on measuring participation, environment, goal setting

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • For Aim 1, participants met the following inclusion criteria: the caregiver is at least 18 years old; reads, writes, and speaks English; has access to broadband internet; resides in the U.S; and has a child between 0 and 3 years old who is receiving services for developmental delay.
  • For Aim 2, caregivers were eligible for inclusion if they: 1) were 18 years or older; 2) spoke and write English; 3) had a child aged 0-5 years old who was receiving rehabilitation services; 4) had broadband internet access; and 5) denoted at least one area of desired change during participation assessment.

Exclusion Criteria:

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    PEM-Plus Group

    Arm Description

    For Aim 1, 6 parents of young children were recruited to perform tasks related to navigating the PEM+ interface. Data on completion rate and time, as well as user satisfaction, were analyzed to guide PEM+ improvements. For Aim 2, we recruited 26 participants to enroll in a feasibility trial of PEM+. Caregivers who completed the YC-PEM e-PRO to evaluate their child's participation clicked on a weblink to begin PEM+, whereby they built on their YC-PEM responses for the purpose of creating a participation-focused care plan to share with their child's rehabilitation team. Caregivers were instructed to complete the PEM+ over a two-week (14 day) period because it mimics what would be provided in routine care.

    Outcomes

    Primary Outcome Measures

    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.
    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
    Percentage of caregivers completing PEM+ independently
    As an indicator of PEM+ feasibility, we used web analytics to estimate proportion of care plans created
    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.
    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.
    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.

    Secondary Outcome Measures

    Full Information

    First Posted
    January 22, 2019
    Last Updated
    January 24, 2019
    Sponsor
    Mary A Khetani
    Collaborators
    McGill University, McMaster University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03820011
    Brief Title
    Participation and Environment Measure-Plus (PEM-Plus) Care Planning Intervention
    Acronym
    PEM-Plus
    Official Title
    Feasibility Test of a Pediatric Web-Based Care Planning Guide
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    July 1, 2016 (Actual)
    Primary Completion Date
    February 1, 2018 (Actual)
    Study Completion Date
    August 1, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Mary A Khetani
    Collaborators
    McGill University, McMaster University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief 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.
    Detailed 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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Developmental Disability, Early Intervention (Education)
    Keywords
    participation, environment, goal setting

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    32 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    PEM-Plus Group
    Arm Type
    Experimental
    Arm Description
    For Aim 1, 6 parents of young children were recruited to perform tasks related to navigating the PEM+ interface. Data on completion rate and time, as well as user satisfaction, were analyzed to guide PEM+ improvements. For Aim 2, we recruited 26 participants to enroll in a feasibility trial of PEM+. Caregivers who completed the YC-PEM e-PRO to evaluate their child's participation clicked on a weblink to begin PEM+, whereby they built on their YC-PEM responses for the purpose of creating a participation-focused care plan to share with their child's rehabilitation team. Caregivers were instructed to complete the PEM+ over a two-week (14 day) period because it mimics what would be provided in routine care.
    Intervention Type
    Other
    Intervention Name(s)
    PEM+
    Intervention Description
    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).
    Primary Outcome Measure Information:
    Title
    Mean retention rates
    Description
    As an indicator of PEM+ feasibility, we used web analytics to obtain estimates of the percentage of caregivers who enrolled completed the trial.
    Time Frame
    Following completion of two-week trial
    Title
    Median PEM+ completion time
    Description
    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
    Time Frame
    Following completion of two-week trial
    Title
    Percentage of caregivers completing PEM+ independently
    Description
    As an indicator of PEM+ feasibility, we used web analytics to estimate proportion of care plans created
    Time Frame
    Following completion of two-week trial
    Title
    Median number of PEM+ care plans created
    Description
    As an indicator of PEM+ feasibility, we used web analytics estimate the number of care plans created over a two-week trial period.
    Time Frame
    Following completion of two-week trial
    Title
    Usefulness, Satisfaction, and Ease of Use Questionnaire (USE)
    Description
    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.
    Time Frame
    Following completion of two-week trial
    Title
    Caregiver Self-Efficacy to Promote Child's Participation in Activities
    Description
    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.
    Time Frame
    Following completion of two-week trial

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: For Aim 1, participants met the following inclusion criteria: the caregiver is at least 18 years old; reads, writes, and speaks English; has access to broadband internet; resides in the U.S; and has a child between 0 and 3 years old who is receiving services for developmental delay. For Aim 2, caregivers were eligible for inclusion if they: 1) were 18 years or older; 2) spoke and write English; 3) had a child aged 0-5 years old who was receiving rehabilitation services; 4) had broadband internet access; and 5) denoted at least one area of desired change during participation assessment. Exclusion Criteria:

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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