Fit Families Program: Fundamental Motor Skill Intervention in Children With Autism Spectrum Disorders and Their Parents

University of Wisconsin (UW)

Status: Completed

Conditions: Autism Spectrum Disorder

Treatments: Behavioral: Physical Activities & Activity Booklets; Other: 12-week FMS Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT04612647

2019-1256

EDUC/KINESIOLOGY/KINESIO (Other Identifier)

A176000 (Other Identifier)

Details and patient eligibility

About

The investigators aim to identify the effect of a 12-week fundamental motor skills (FMS) (e.g., throwing, catching, running) intervention on the active participation in physical recreation activities and a variety of other factors (child behaviors, communication, and adaptive skills) and to identify patterns, benefits, constraints, and strategies to active participation in physical recreation activities among families of children with autism spectrum disorders (ASD) (pre-post) through in-person or via phone interviews with parents and children with ASD.

Full description

Participants will be randomly assigned to one of three protocols: 1) Workshop group, 2) Home-based group, and 3) wait-listed home-based group. Participants in all groups will receive an activity booklet and physical education-related activity items (e.g., ball, hoop). The hypothesis is that both the workshop and home-based groups will improve in all measures from pre to post compared to the wait-list control group. The investigators want to determine if the differences in the workshop and home-based groups differ significantly or are equitable in terms of gains in all areas.

Note: Due to COVID-19 for the post-test, instead of parents attending the UW-Facilities, they will be asked to videotape themselves and their children while performing the test of gross motor development (TGMD) activities. For the follow-up test (Fall 2020) we will expect to conduct these in person. However, if the situation due to COVID-19 remains the same, the investigators will ask families to follow the same procedures (videotape themselves and their children).

Enrollment: 41 patients

Sex: All

Ages: 4 to 11 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Parents (one per family) and children with ASD ages 4 to 11 will be included (recruited as a dyad).

Inclusion Criteria:

• ASD must be the primary disability of the child
• Children will be considered to have ASD if they score above the clinical cutoff or 15 on both the lifetime and current versions of the SCQ. Diagnostic severity of ASD will not be a factor in recruitment.
• Children must be able to participate in the program activities.
• Children must be ambulatory and able to follow verbal or picture directions with support
• Children with significant communication needs will still be considered for the study
• No age restriction for adults (parents of children with ASD)
• Parents should be ambulatory and not have any restriction to do physical activity

Exclusion Criteria:

• Parents of children with other primary disabilities, or parents who do not have children with ASD will be excluded.
• Participants cannot exhibit aggressive behavior
• Children who are non-ambulatory, or participants (children) with significant behavioral or sensory impairments will also be excluded based on application information, including existing behavior intervention plans and existing school information

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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41 participants in 3 patient groups

Workshop group

Experimental group

Description:

Participants in the workshop group will be offered four one-day workshops (3-hours each) covering topics of 1) Sensory Integration, 2) Communication, 3) Aquatic Opportunities, and 4) Physical activity and Sports (during intervention)-\[Parents and Children-Workshop Group\]. In addition to the workshops, this group and the home-based group will receive information (activity booklets) and physical education (physical activity)-related equipment.

Treatment:

Behavioral: Physical Activities & Activity Booklets

Other: 12-week FMS Intervention

Home-based group

Experimental group

Description:

Participants in the home-based group will not participate in the four half-day workshops, but they will receive the same information (activity booklets) and physical activity equipment as the workshop group (during intervention)-\[Parents and Children-Home Group\].

Treatment:

Behavioral: Physical Activities & Activity Booklets

wait-listed home-based group

No Intervention group

Description:

Wait-list home-based group will serve as the control group (during intervention)-\[Parents and Children-Control Group\]. This group will be instructed to continue their typical routines and activities for the duration of the intervention. They will be asked to attend the pre and posttest, as well as a follow up three weeks and 3 months after the completion of the 12-week period. Immediately following the follow-up test (3 months after the intervention), participants in the wait-list home-based group will be offered the home-based program (e.g., receiving the same intervention protocol and materials (physical education equipment and lesson plans/workbook) following all procedures as described for that group previously.