PLAY-LONG: PLAY LONG: The Effect of Sports and Recreation Participation for Young chiLdren With physicAl disabilitY

Sponsor
Allina Health System (Other)
Overall Status
Terminated
CT.gov ID
NCT03256318
Collaborator
(none)
16
1
28.7
0.6

Study Details

Study Description

Brief Summary

Ten year longitudinal survey following children with disabilities who have participated in Sports and Recreation from a young age (5 to 10), and the parents of children who have participated in Sports and Recreation at a young age (5 to 10). These children will be followed for 10 years with surveys every 6 months, whether they are currently participating in sports and recreation activities or not.

The purpose of this longitudinal study is to examine the effects of early participation in organized sports and recreation activities (S&R) on self-reported health and health-related quality of life of children and youth (C&Y) with disabilities and their parent-reported social participation. This project will examine child and parent reported differences between:

  1. C&Y with disabilities who participate in S&R and those who have discontinued participation in S&R programs

  2. C&Y with disabilities who participate in sports vs. those who participate in recreation, and

  3. C&Y with disabilities who participate in S&R and normative data on C&Y with disabilities and those without disabilities.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational
Actual Enrollment :
16 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
PLAY LONG: The Effect of Sports and Recreation Participation for Young chiLdren With physicAl disabilitY - Longitudinal Study
Actual Study Start Date :
Aug 30, 2017
Actual Primary Completion Date :
Jan 21, 2020
Actual Study Completion Date :
Jan 21, 2020

Arms and Interventions

Arm Intervention/Treatment
Children in Sports and Rec

Children with disabilities who enter the study between ages 5 and 10 who are participating in a Sports and Recreation Program. They will receive no intervention, only surveys.

Other: No intervention
No intervention; surveys/questionnaires only

Comparison Children

Children with disabilities who enter the study between ages 5 and 10 and end participation in Sports and Recreation Program at a later date. They will receive no intervention, only surveys.

Other: No intervention
No intervention; surveys/questionnaires only

Outcome Measures

Primary Outcome Measures

  1. Change in health related quality of life [Every 6 months for 10 years.]

    As measured by KIDSCREEN-10 questionnaire

Secondary Outcome Measures

  1. Change in general health [Every 6 months for 10 years.]

    Self reported general health as measured by PROMIS Pediatric Global Health Measure

  2. Change in social participation [Every 6 months for 10 years.]

    Self reported (or parent-reported) social participation as measured by PROMIS Pediatric Global Health Measure

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • At the time of enrollment, the child must be between the ages of 5 and 10 and be participating in an adapted sports and recreation program.

  • At the time of enrollment, the parent must have a child between the ages of 5 and 10, who is participating in an adapted sports and recreation program.

  • Children and parents who are enrolled in the study will continue to participate in the study for 10 years.

Exclusion Criteria:
  • Children who are younger than 5 or older than 10 will not be entered into the study, nor will parents whose children are younger than 5 or older than 10 be entered into the study. .

  • Individuals who do not read and write in English will be excluded from the study.

  • Children who are wards of the state, or in foster care will be excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Courage Kenny Rehabilitation Institute Golden Valley Minnesota United States 55422

Sponsors and Collaborators

  • Allina Health System

Investigators

  • Principal Investigator: Nancy Flinn, PhD, OTR/L, Allina Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nancy Flinn, Senior Scientific Advisor, Allina Health System
ClinicalTrials.gov Identifier:
NCT03256318
Other Study ID Numbers:
  • CKNF-1701
First Posted:
Aug 22, 2017
Last Update Posted:
Feb 6, 2020
Last Verified:
Feb 1, 2020
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

Study Results

No Results Posted as of Feb 6, 2020