Living Well With a Disability Curriculum Adaptation Evaluation Plan

The purpose of this proposal is to implement a joint project with Georgia Southern University and the Effingham County Navigator Team to improve the quality of life of families with a child with a disability in southeast Georgia. The final outcome of this project will be a new curriculum, Living Well Together, which builds on a previous implementation of the Living Well with a Disability curriculum in Bulloch County.

Study Overview

• Status: Completed
• Conditions: Developmental Disabilities; Health Education; Community Health Services; Health Services for Persons With Disabilities
• Intervention / Treatment: Behavioral: Living Well with a Disability

Detailed Description

First, parent facilitators will be recruited and matched with their peers. Parent facilitators will be members of the Effingham County Navigator Team with a child with a disability. The peer matching resembles the community lay health worker model. The community lay health worker model will reduce the amount of time needed to meet face to face with families. To begin adapting the facilitator training and curriculum, the program directors will work with representatives from the University of Montana Rural Institute on Disabilities to review and update training materials. A representative from the Rural Institute on Disabilities will deliver an online intensive facilitator training. The facilitator training is approximately 15 hours long. The training includes three major components: peer training, facilitator training, and Master "Train the Trainer" training. The project directors will work with the Effingham County Navigator Team to recruit parents. The Navigator Team will recruit five parents as parent facilitators. The parents will work together with the project directors to deliver the adapted curriculum to participating families. With bi-weekly meetings for 10 weeks between parent facilitators and family participants in the home or another desired location. The project directors have already participated in the facilitator training and will serve as mentors to newly trained facilitators. At the end of the online training session, the parent facilitators will be equipped to successfully implement the Living Well curriculum. The project directors will schedule a working meeting before and after the facilitator training to discuss curriculum changes with the Rural Institute on Disabilities representative. Changes in readability are anticipated since the target audience includes adolescents. Curriculum delivery methods will need tailoring to match a family-based approach including activities to be completed at the home at the family and individual levels for parents, siblings, and children. Both GSU faculty and the Navigator team will lead monthly summary meetings to review the adapted content. These meetings will take place at a convenient location in the community as determined by the Navigator team. Pre and post focus groups will take place before and after these monthly meetings at a convenient locale in the community.

• Study Type: Interventional
• Enrollment (Actual): 39
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Georgia
    • Springfield, Georgia, United States, 31329
      • B and B Care Services

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 3 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria

Families of with a child (3-50) with any developmental disability

Exclusion Criteria

Family and child are unable to follow directions and participate in curriculum activities.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Living Well with a Disability; The parents will work together with the project directors to deliver the adapted curriculum to participating families. With bi-weekly meetings for 10 weeks between parent facilitators and family participants in the home or another desired location. The project directors have already participated in the facilitator training and will serve as mentors to newly trained facilitators. At the end of the online training session, the parent facilitators will be equipped to successfully implement the Living Well curriculum.

Behavioral: Living Well with a Disability; Implementation of an adapted health promotion program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Global Health	Patient Reported Outcomes Measurement Information System Parent Proxy scale v 1.0 Global Health; Patient Reported Outcome Measurement Information System (PROMIS) Pediatric Global Health (PROMIS PGH-7) measures general health, quality of life, physical health, mental health, feeling sad, social health (fun with friends), and parents listening to ideas.; Each item is measured on a likert scale from 1 (never) to 5 (always). There is one item for each subscale listed above. A range for each subscale would be 1-5. Typically, results are reported as a whole so the range would be 7 to 35.; For each subscale and the scale as a whole the higher the score, the better the global health.; Subscales are summed to compute the total score.	12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Family Relationships	Patient Reported Outcomes Measurement Information System Parent Proxy scale v. 1.0 Family Relationships; The Family Relationships subscale measures the importance and strength of the family unit perceived by the child in the past four weeks.; Each item is measured on a Likert scale from 1 (never) to 4 (always). There are four items in this subscale. The reports are reported as a whole so the range is 4 to 16.; The higher the score, the stronger the family relationships.; Items are summed for the total score.	12 months
Life Satisfaction	Patient Reported Outcomes Measurement Information System Parent Proxy scale v 1.0 Life Satisfaction; The Life Satisfaction subscale measures quality of life in the past four weeks.; Each item is measured on a Likert scale from 1 (not at all) to 5 (very much). There are eight items in this scale. The range for the whole subscale is 8-40.; The higher the score, the better quality of life.; Each item is summed for the total score.	12 months
Physical Activity	Patient Reported Outcomes Measurement Information System Parent Proxy scale v 1.0 Physical Activity; The Physical Activity subscale reports frequency and intensity of exercise of the child in the past week.; Each item is measured on a Likert scale from 1 (no days) to 5 (6-7 days). There are eight items in this subscale. The total range is 8 (no exercise) to 40 (exercising regularly).; The higher the score, the more physically active the individual is.; The items are summed together for the score.	12 months
Psychological Stress Experiences	Patient Reported Outcomes Measurement Information System Parent Proxy scale v 1.0 Psychological Stress Experiences	12 months
Peer Relationships	Patient Reported Outcomes Measurement Information System Parent Proxy scale v 1.0 Peer Relationships; The Peer Relationships subscale measures the child's social activity in the last 7 days.; Each item is measured on a Likert scale from 1 (never) to 5 (almost always). There are 7 items in the scale. The range is 7 (doesn't interact with friends) to 35 (very socially active).; The higher the score the better the relationships.; The items are summed together for a total score.	12 months

Collaborators and Investigators

• Sponsor: Georgia Southern University
• Investigators: Principal Investigator: Gavin Colquitt, EdD, Georgia Southern University

Study record dates

Study Major Dates

• Study Start (Actual): March 24, 2018
• Primary Completion (Actual): January 15, 2022
• Study Completion (Actual): January 15, 2022

Study Registration Dates

• First Submitted: January 31, 2018
• First Submitted That Met QC Criteria: February 25, 2018
• First Posted (Actual): February 27, 2018

Study Record Updates

• Last Update Posted (Actual): September 15, 2023
• Last Update Submitted That Met QC Criteria: September 14, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Neurodevelopmental Disorders; Developmental Disabilities
• Other Study ID Numbers: H18234

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No