Developmental Disability Clinical Trial
— PEM-PlusOfficial title:
Feasibility Test of a Pediatric Web-Based Care Planning Guide
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 |
Verified date | April 2024 |
Source | University of Illinois at Chicago |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Mary A Khetani | McGill University, McMaster University |
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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