ASSISTS: App for Strengthening Services In Specialized Therapeutic Support

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT05207956
Collaborator
(none)
27
1
2
9.4
2.9

Study Details

Study Description

Brief Summary

In partnership with a digital health software company, the University research team created two versions of a mobile application to help behavioral health technicians (BHT's) who work with students with autism collect data. The first version comprises a basic electronic platform for data collection. The second version has the same basic electronic platform for data collection, plus additional features designed to increase motivation to collect data and ease the burden of data collection.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behavioral economics strategies
  • Other: Electronic platform
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
27 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
After consenting to participate in the trial, participants will be randomized in pairs to one of the two study arms.After consenting to participate in the trial, participants will be randomized in pairs to one of the two study arms.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
App for Strengthening Services In Specialized Therapeutic Support
Actual Study Start Date :
Sep 9, 2021
Actual Primary Completion Date :
Jun 21, 2022
Actual Study Completion Date :
Jun 21, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Enhanced Electronic Platform

A basic electronic platform for data collection that contains additional features designed to increase motivation to collect data and ease of data collection.

Behavioral: Behavioral economics strategies
Behavioral economics features designed to increase motivation to collect data and ease of data collection on the electronic platform.

Other: Electronic platform
Electronic platform to collect data

Active Comparator: Electronic Platform Not Enhanced

A basic electronic platform for data collection.

Other: Electronic platform
Electronic platform to collect data

Outcome Measures

Primary Outcome Measures

  1. The average difference in hourly data collection between groups across three weeks [Three-week trial period]

    Measure of frequency paraprofessionals collect hourly interval data with children during each school day, across a three week period.

Secondary Outcome Measures

  1. Theory of Planned Behavior Questionnaire [Assessed at baseline and 3 weeks after enrollment]

    Theory of Planned Behavior Questionnaire: A measure of participant's intentions to collect data as measured on a 7-point Likert scale from "strongly disagree" to "strongly agree". The questionnaire is 7 questions and measures intentions, attitude, perceived norms, and self-efficacy. There is no better or worse outcome measured by the scale, only intentions to implement the intervention.

  2. System Usability Scale [Assessed at baseline and 3 weeks after enrollment]

    System Usability Scale: A validated measure of the usability and satisfaction with a specific technology. Measured by answering 10 questions on a 5-point Likert scale from "strongly disagree" to "strongly agree". There is no better or worse outcome measured by the scale, only intentions to implement the intervention.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Participants must be working as a paraprofessionals or behavioral health technicians

  • Currently providing individual support to children with autism

  • Currently providing services in Philadelphia preschools, schools, day cares, or homes.

Exclusion Criteria:
  • n/a

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pennsylvania Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • University of Pennsylvania

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT05207956
Other Study ID Numbers:
  • 849995
First Posted:
Jan 26, 2022
Last Update Posted:
Jul 28, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Pennsylvania
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2022