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Clinical Trials/NCT04173871
NCT04173871UnknownNot Applicable

Effects of Systematic Proprioceptive-tactile Stimulation With Use of the Protac MyFit®

University of Southern Denmark2 sites in 1 country240 target enrollmentStarted: April 1, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
240
Locations
2
Primary Endpoint
Test of Everyday Attention - Children (TEA-Ch)

Study Overview

Brief Summary

Children with sensory impairment (SPD) are often unable to sit still and focus their attention. This can affect the children by limiting their opportunities for participation in school activities. Previous studies indicate a link between childhood SPD, childhood anxiety, and obsessive-compulsive disorder (OCD) in adulthood. Research and clinical experience suggest that systematic use of proprioceptive-tactile stimulant aids may have a positive effect for children with SPD.

The aim of the project is to investigate and describe the effects of a systematic use of proprioceptive-tactile stimulating vest, MyFit®, for children 6-12 years with SPD in the form of sensory-seeking behaviour.

Research questions:

  • Can systematic use of MyFit® for children with sensory seeking behaviour increase their participation in school activities?
  • Can systematic use of MyFit® support children with sensory seeking behaviour to increase their awareness, concentration and focus on tasks?
  • Can systematic use of MyFit® affect children's feelings of confidence and self-efficacy? The project seeks to answer these questions to contribute to knowledge on how children with sensory seeking behaviours can be supported for better participation in school activities.

The study will be a randomized controlled trial of 240 children with SPD and sensory seeking behaviour.

Detailed Description

The purpose of the study is to investigate the effect of systematic proprioceptive-tactile stimulation through use of the Protac MyFit® to children, age 6-12 years with SPD and sensory seeking behavior. The primary objective is to determine the effect of the vest on the children´s abilities for attention and participation in school activities, and secondary their abilities for on-task behavior and feelings of self-esteem and self-efficacy.

Method & design The study is a randomized controlled trial (RCT), were primary school children with SPD and sensory seeking behavior receives an intervention with systematic proprioceptive-tactile stimulation through use of the Protac MyFit®.

Study setting and participants The study will be conducted in public primary schools across Denmark. Participants will be 240 children with SPD and sensory seeking behaviour age 6-12 years attending public primary school. Sample size has been calculated based on results from the feasibility study and the primary outcome of sustained attention measured with the Test of Every Day Attention-Children. The sample size is calculated with Ancova analysis and made with an anticipated difference on 1.5 with a correlation of .07 and a standard deviation at 5.

Recruitment and randomization Recruitment will be conducted in collaboration with gatekeepers from municipal Pedagogical Psychological Counselling (PPR) departments and public-school managements across Denmark, that will assist in identifying possible study participants. Parents to possible participants will be introduced to the study by the gatekeepers and handed out written information about the study together with a baseline questionnaire, the Short Sensory Profile questionnaire (SSP), a consent form for participation and a franked reply envelope.

The included children will be randomized into two groups; an intervention group (A) and a control group (B). The randomization will be computer generated 1:1. Additionally, 20 of the included children will be strategically selected (as per age, gender, group) to represent the main population and complete a qualitative research interview regarding their experiences of using the MyFit®.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
6 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Children age 6-12 years, with SPD and sensory seeking behaviour as identified by the SSP, attending primary school.

Exclusion Criteria

  • Children with mental retardation or other massive cognitive impairment, and children who use corset or molded wheelchairs.

Outcomes

Primary Outcomes

Test of Everyday Attention - Children (TEA-Ch)

Time Frame: 21 days

TEA-Ch is a normed and standardised battery of 9 tests, that examines the child's ability for three different types of attention (selective attention, sustained attention and attentional control/switching)

Child Occupational Self Assessment (COSA)

Time Frame: 21 days

COSA is an assessment tool designed to capture children´s perceptions of their own occupational competence together with their rating of importance of everyday activities.

Secondary Outcomes

  • Registration of on-task-behaviour(21 days)
  • Five to fifteen (FTF)(21 days)
  • Strengths and Difficulties Questionnaire (SDQ)(21 days)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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