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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05473247
Other study ID # STUDY00148828
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 15, 2023
Est. completion date August 30, 2030

Study information

Verified date October 2022
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are assessing acceptability, appropriateness, and feasibility of the adapted GameSquad-DS intervention using validated scales alongside qualitative data among young adults with Down Syndrome. Specifically, the investigators will assess mins/wk of Ring-Fit Adventure played, attendance at 30 min. virtual health coaching sessions, semi-structured interviews, participant retention, and intervention safety measured as number of adverse events.


Description:

Adults with DS face unique barriers to participation in MVPA. Exergames, which integrate MVPA into video game play are an affordable, accessible, home-based exercise program which has shown effectiveness for increasing MVPA and improving both physical and cognitive function in typically developed populations. An exergaming intervention with individual health coaching called GameSquad has been shown to be effective in improving MVPA and cardiometabolic parameters in children with overweight/obesity and adolescents with neurodevelopmental and psychiatric diagnoses. The investigators propose a two phased project to adapt/evaluate the GameSquad intervention for use in adults with DS (GameSquad-DS). In Phase 1, the investigators will utilize a formative approach to develop GameSquad-DS, pilot test the intervention for 4 weeks in 10 young adults with DS and use feedback to refine the intervention for use in Phase 2. In Phase 2, the investigators will conduct a 12-wk. single arm pilot trial in 20 young adults with DS to assess the acceptability, appropriateness, and feasibility of the intervention and calculate effect sizes for change MVPA, physical function, muscular strength, physical activity enjoyment, and self-efficacy. Successful completion of this project represents an initial step in achieving the goal of developing effective interventions to increase MVPA and promote healthy aging in adults with DS.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 30, 2030
Est. primary completion date June 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Young adults (18-30 yrs.). - Diagnosis of DS. - Sufficient functional ability to understand directions, communicate preferences, wants, and needs through spoken language. - Living at home with a parent/guardian or in a supported living environment with a parent/caregiver who agrees to serve as a study partner. Exclusion Criteria: - Unable to participate in MVPA. - Serious medical risk, e.g., cancer, recent heart attack, stroke, angioplasty as determined by their primary care provider (PCP).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Ring-Fit Adventure Group
Participants will be asked to play the exergame software, Ring-Fit Adventure, and attend weekly virtual health coaching sessions.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Kansas Medical Center HRSA/Maternal and Child Health Bureau

Outcome

Type Measure Description Time frame Safety issue
Primary Minutes of Gameplay per week Minutes of Ring-Fit Adventure played per week will be collected from a self-reported sign in sheet. 12-weeks
Primary Retention Participant retention will be collected. 12-weeks
Primary Attendance Attendance at 30 min virtual health coaching sessions will be collected. 12-weeks
Secondary 6-minute walk test This test measures the distance that a participant can walk on a flat, hard surface in a period of 6 minutes. The research team will instruct them on how to prepare and conduct this test. 12-weeks
Secondary Leg Strength Leg strength will be measured on the leg press machine. Researchers will assess the maximum amount of weight the participant can press for 5 repetitions. 12-weeks
Secondary Hand Grip Strength The participant will be asked to squeeze a device as hard as they can to test their grip strength. This will be done on both hands. 12-weeks
Secondary Timed Up and Go During this test, the participant will be asked to sit down in a chair. Approximately 10 feet in front of the participant there will be a line on the floor. The research team will say "go" and the participant will get up from the chair, walk to the line at a normal pace, and then turnaround and walk back to the chair and sit down again. The research team will record how long it takes to do this. 12-weeks
Secondary Balance During this test, the investigators will ask the participant to balance on one leg and reach in three directions as far as they can with their other foot. They will then do the same on the other leg. 12-weeks
Secondary Adverse Events Adverse events will be collected. 12-weeks
Secondary Qualitative Interview Data Semi-Structured interviews will occur after the 12-week intervention to allow participants to make sense of their experience in the intervention. 12-weeks
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