Multi Sensory Stimulation And Priming (MuSSAP) in Infants at Risk of Unilateral Cerebral Palsy (MuSSAP)

October 27, 2022 updated by: Sint Maartenskliniek

Multi Sensory Stimulation And Priming (MuSSAP) in Infants (4-12 Months of Age) at Risk of Developing Unilateral Cerebral Palsy (uCP)

A pilot randomized clinical trial exploring the effect of a Multi Sensory Stimulation And Priming (MuSSAP) training on improving manual ability in infants at risk of developing unilateral Cerebral Palsy.

Study Overview

Detailed Description

Rationale:

Unilateral Cerebral Palsy (uCP) results from early brain damage. In adults, brain damage in one side of the (pre) motor cortex is associated with functional problems in the contralateral side of the body and vice versa. This is related to extensive crossings of the descending corticospinal tracts connecting the central motor systems with the musculature of the extremities. However, during the first years of our lives, crossings of the corticospinal tracts are less defined and the motor system relies on both ipsi- and contralateral connections to control the extremities. In children with uCP the classical development and strengthening of the crossed connections of the corticospinal tracts might be hampered. Although reorganization with ipsilateral corticospinal tracts can mediate useful hand function, patients with the most favourable functional outcome retain crossed projections from the affected hemisphere. To facilitate maturation of the corticospinal tracts, it seems crucial to start early with intervention at the stage that the corticospinal tracts show high plasticity. Attention benefits from multisensory congruent signals, particularly if this congruency involves rhythmical similarity. Attention influences the sensitivity of neurons to detect sensory activity and the ability of neurons to detect sensory stimulation. Formation of neural pathways is facilitated by increasing activity in (new) functional neural circuits. During the multisensory stimulation, motor actions of both or one arm and hand will be provoked. In contrast to the functional training focused primarily on motor output, MuSSAP enhances motor learning by stimulating the perception-action loop. In this study, we propose to pilot test whether a new intervention; Multi Sensory Stimulation And Priming (MuSSAP) can be applied in clinical practice in infants 4-12 months of age with diagnosed unilateral cerebral damage having increased risk on the development of unilateral cerebral palsy.

Objective:

Primary objective: The following hypothesis will be tested: MuSSAP in infants 4-12 months of age with diagnosed unilateral cerebral damage, is a feasible protocol and results in an enhanced motor development as compared to Intensive Usual Care (Upper Limb).

Secondary Objective(s): Assessment of feasibility of the intervention: Can the MuSSAP intervention and procedures be successfully executed and delivered to the participants? Assessment of acceptability: Suitability of the intervention and the study procedures from the perspective of the participants. Determining effect sizes for a future full-scale randomized clinical trial and clinical relevance.

Study design:

The study is designed as a pilot randomized clinical trial (RCT) with three measuring moments (before intervention, after intervention, and follow-up).

Study population:

The study population consists of 16 infants at risk for developing unilateral cerebral palsy. These infants will either be born preterm suffering from unilateral periventricular haemorrhagic infarction, or born at term suffering from unilateral middle cerebral artery (MCA) stroke. The infants at risk will be allocated either to the MuSSAP intervention group (8 infants) or the Intensive Usual Care (Upper Limb) group (8 infants) by randomisation. Data of 8 typically developing infants will be used to monitor typical development of infants of 4-12 months old.

Intervention:

Both the MuSSAP and the Intensive Usual Care (Upper Limb) interventions are home based and consist of 30 minutes (divided in 3 periods of 10 minutes each) of remediating impairments practicing specific age related movements and skills, each day for an 8-week period, conducted by the parents and once a week by a physical or occupational therapist in the home environment. Upper extremity motor activities like reaching, grasping and holding are practiced. Coaching of parents and therapists will be performed by the occupational therapist of the Sint Maartenskliniek. This will be realised through analysing video recordings of the intervention in the home environment once a week.

Multi Sensory Stimulation And Priming (MuSSAP): In the MuSSAP intervention a custom made wristband will be used to provide rhythmical congruent multisensory stimulations to the affected arm and hand aiming to increase attention for the affected upper limb. Subsequently, motor actions of the affected arm and hand will be provoked.

Intensive Usual Care (Upper Limb): This intervention is a more intensive (in duration and frequency) version of standard Usual Care with focus on the motor development of the affected upper extremity.

In both intervention groups infants will additionally receive pediatric physical therapy in the home environment (usual care) focusing on gross motor development.

Primary study parameters/outcome of the study:

The primary study parameter aims at development of handfunction/ manual ability (measured with the Hand Assessment for Infants (HAI)).

Study Type

Interventional

Enrollment (Actual)

24

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

3 years to 2 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria Intervention:

  • Born preterm suffering from unilateral periventricular haemorrhagic infarction with involvement of the corticospinal tracts
  • Born term suffering from unilateral middle cerebral artery stroke with involvement of the corticospinal tracts
  • ±4 months of age (time the infant starts to reach with at least one hand) to 10 months of age (age corrected in case of prematurity)

Exclusion Criteria Intervention:

  • Severe epilepsy
  • Severe sensory impairments (blindness, deafness)
  • Children with clinical signs of bilateral involvement
  • Inability of parents to respond to interviews or questionnaires in Dutch
  • Expected inability of parents to adhere to the home-based protocol

Inclusion Criteria age matched typical developing infants:

  • Born term (≥37 weeks gestational age)
  • Birth weight within a normal range (≥2500 grams)

Exclusion Criteria age matched typical developing infants:

  • Inability of parents to respond to interviews or questionnaires in Dutch
  • Expected inability of parents to adhere to planned measuring moments

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Multi Sensory Stimulation And Priming
8 weeks, 30 minutes per day home based MuSSAP training.
In the MuSSAP intervention group, the infant wears a multisensory stimulating wristband aiming at increasing attention for the affected upper limb and readiness to initiate a goal-directed movement. Parents are instructed to present a toy to their child if the child shows attention to the affected arm and hand. Upper extremity motor activities like reaching, grasping and holding are practiced. Parents practice daily and once a week the training will be guided or conducted by a physical or occupational therapist in the home environment. An occupational therapist from the rehabilitation center will coach parents during the intervention period through the internet, by means of analyzing the videos from the home training.
Experimental: Intensive Usual Care (Upper Limb)
8 weeks, 30 minutes per day home based Intensive Usual Care (Upper Limb).
The Intensive Usual Care (Upper Limb) intervention is a more intensive (in duration and frequency) version of standard Usual Care with focus on the motor development of the affected upper extremity. Upper extremity motor activities like reaching, grasping and holding are practiced. Parents practice daily and once a week the training will be guided or conducted by a physical or occupational therapist in the home environment. An occupational therapist from the rehabilitation center will coach parents during the intervention period through the internet, by means of analyzing the videos from the home training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean change from T0 in manual ability as assessed by the Hand Assessment for Infants (HAI)
Time Frame: T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
The HAI is intended to evaluate the quality of goal-directed manual actions in infants, 3-12 months of age, at risk of developing unilateral CP. The test procedure comprises a semi-structured video-recorded 10-15-min play session. HAI is intended to detect and quantify possible asymmetry between hands by providing scores for each hand separately (Each Hand sum Score (EaHS) (range 0-24)), and to provide a measure of bilateral hand use (Both Hands Measure (BoHM) (range 0-100)) with a higher score reflecting a better outcome.
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Adherence based on total training time
Time Frame: During 8 week intervention
Parents fill out a digital time registration form to assess intervention adherence every day. Adherence will be calculated by dividing the registrated total training time by total planned training time (28 hours).
During 8 week intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Motor development as assessed by the Bayley Scales of Infant and Toddler Development - Third Edition (Dutch version) (Bayley-III-NL)
Time Frame: T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
The motor scale of the Bayley-III-NL will be used to assess motor development. The gross motor (GM) subscale raw scores (range 0-72) will be determined on all assessment points, the fine motor (FM) subscale raw scores (range 0-66) on T0 only. A higher score reflects a better outcome.
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Gross motor development as assessed by the Gross Motor Function Measure (GMFM)
Time Frame: T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
The GMFM contains eighty-eight items grouped into five dimensions (e.g. lying and rolling, sitting, crawling and kneeling, standing, walking, running and jumping) and is sensitive to motor developmental changes over time.
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Quality of life as assessed by the Infant and Toddler Quality of life Questionnaire (ITQOL)
Time Frame: T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
The infant/toddler quality of life questionnaire (ITQOL) is a generic parent-completed 'profile-measure' for health status and health-related quality of life of children between 2 months and 5 years old. Raw scale scores are transformed to a standardized 0-100 continuum with a higher score reflecting a better health status.
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Reaction time of self-initiated goal-directed movement and attention as assessed by the Video Observation Attention Affected Hand (VOAAH)
Time Frame: During 8 week intervention
The VOAAH is a video-observation tool that is used to assess time to self-initiated goal-directed movement and time to attention. Training session videos recorded by parents are manually scored using a standardized protocol.
During 8 week intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Pauline Aarts, PhD, Sint Maartenskliniek

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 14, 2016

Primary Completion (Actual)

August 20, 2018

Study Completion (Actual)

August 20, 2018

Study Registration Dates

First Submitted

September 5, 2022

First Submitted That Met QC Criteria

September 5, 2022

First Posted (Actual)

September 9, 2022

Study Record Updates

Last Update Posted (Actual)

October 31, 2022

Last Update Submitted That Met QC Criteria

October 27, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

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

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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