Multi Sensory Stimulation And Priming (MuSSAP) in Infants at Risk of Unilateral Cerebral Palsy (MuSSAP)
Primary Purpose
Unilateral Cerebral Palsy
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Multi Sensory Stimulation and Priming
Intensive Usual Care (Upper Limb)
Sponsored by
About this trial
This is an interventional treatment trial for Unilateral Cerebral Palsy focused on measuring Cerebral Palsy, Multisensory Stimulation, Hand function, Infants, Early intervention
Eligibility Criteria
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
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Multi Sensory Stimulation And Priming
Intensive Usual Care (Upper Limb)
Arm Description
8 weeks, 30 minutes per day home based MuSSAP training.
8 weeks, 30 minutes per day home based Intensive Usual Care (Upper Limb).
Outcomes
Primary Outcome Measures
Mean change from T0 in manual ability as assessed by the Hand Assessment for Infants (HAI)
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.
Adherence based on total training time
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).
Secondary Outcome Measures
Motor development as assessed by the Bayley Scales of Infant and Toddler Development - Third Edition (Dutch version) (Bayley-III-NL)
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.
Gross motor development as assessed by the Gross Motor Function Measure (GMFM)
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.
Quality of life as assessed by the Infant and Toddler Quality of life Questionnaire (ITQOL)
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.
Reaction time of self-initiated goal-directed movement and attention as assessed by the Video Observation Attention Affected Hand (VOAAH)
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.
Full Information
NCT ID
NCT05533476
First Posted
September 5, 2022
Last Updated
October 27, 2022
Sponsor
Sint Maartenskliniek
1. Study Identification
Unique Protocol Identification Number
NCT05533476
Brief Title
Multi Sensory Stimulation And Priming (MuSSAP) in Infants at Risk of Unilateral Cerebral Palsy
Acronym
MuSSAP
Official Title
Multi Sensory Stimulation And Priming (MuSSAP) in Infants (4-12 Months of Age) at Risk of Developing Unilateral Cerebral Palsy (uCP)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
June 14, 2016 (Actual)
Primary Completion Date
August 20, 2018 (Actual)
Study Completion Date
August 20, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sint Maartenskliniek
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
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)).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unilateral Cerebral Palsy
Keywords
Cerebral Palsy, Multisensory Stimulation, Hand function, Infants, Early intervention
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Multi Sensory Stimulation And Priming
Arm Type
Experimental
Arm Description
8 weeks, 30 minutes per day home based MuSSAP training.
Arm Title
Intensive Usual Care (Upper Limb)
Arm Type
Experimental
Arm Description
8 weeks, 30 minutes per day home based Intensive Usual Care (Upper Limb).
Intervention Type
Behavioral
Intervention Name(s)
Multi Sensory Stimulation and Priming
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Intensive Usual Care (Upper Limb)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Mean change from T0 in manual ability as assessed by the Hand Assessment for Infants (HAI)
Description
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.
Time Frame
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Title
Adherence based on total training time
Description
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).
Time Frame
During 8 week intervention
Secondary Outcome Measure Information:
Title
Motor development as assessed by the Bayley Scales of Infant and Toddler Development - Third Edition (Dutch version) (Bayley-III-NL)
Description
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.
Time Frame
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Title
Gross motor development as assessed by the Gross Motor Function Measure (GMFM)
Description
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.
Time Frame
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Title
Quality of life as assessed by the Infant and Toddler Quality of life Questionnaire (ITQOL)
Description
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.
Time Frame
T0 (before the start of the intervention), T1 (after the 8-week intervention), T2 (8 weeks after the interventions stops)
Title
Reaction time of self-initiated goal-directed movement and attention as assessed by the Video Observation Attention Affected Hand (VOAAH)
Description
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.
Time Frame
During 8 week intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Months
Maximum Age & Unit of Time
10 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pauline Aarts, PhD
Organizational Affiliation
Sint Maartenskliniek
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35768858
Citation
Verhaegh AP, Nuijen NB, Aarts PB, Nijhuis-van der Sanden MWG, Willemsen MA, Groen BE, Vriezekolk JE. Parents' experiences with a home-based upper limb training program using a video coaching approach for infants and toddlers with unilateral cerebral palsy: a qualitative interview study. BMC Pediatr. 2022 Jun 29;22(1):380. doi: 10.1186/s12887-022-03432-w.
Results Reference
background
Links:
URL
https://www.toetsingonline.nl/to/ccmo_search.nsf/fABRpop?readform&unids=2005C3E3527D170FC1258611001B9157
Description
Medical Ethical Registration and Reviewing form
URL
https://www.maartenskliniek.nl/kinderzorg/kinderrevalidatie/arm-en-handrevalidatie-voor-baby-s-en-peuters
Description
Website information infant and toddler upper limb rehabilitation programs Sint Maartenskliniek
Learn more about this trial
Multi Sensory Stimulation And Priming (MuSSAP) in Infants at Risk of Unilateral Cerebral Palsy
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