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The Sensor Technology and Rehabilitative Timing (START) Protocol: A Randomized Controlled Trial for the Rehabilitation of Mild Traumatic Brain Injury.

Identifieur interne : 000032 ( Main/Exploration ); précédent : 000031; suivant : 000033

The Sensor Technology and Rehabilitative Timing (START) Protocol: A Randomized Controlled Trial for the Rehabilitation of Mild Traumatic Brain Injury.

Auteurs : Lucy Parrington [États-Unis] ; Deborah A. Jehu [Canada] ; Peter C. Fino [États-Unis] ; Samuel Stuart [Royaume-Uni] ; Jennifer Wilhelm [États-Unis] ; Natalie Pettigrew [États-Unis] ; Charles F. Murchison [États-Unis] ; Mahmoud El-Gohary [États-Unis] ; Jess Vanderwalker ; Sean Pearson ; Timothy Hullar [États-Unis] ; James C. Chesnutt [États-Unis] ; Robert J. Peterka ; Fay B. Horak ; Laurie A. King [États-Unis]

Source :

RBID : pubmed:31951263

Descripteurs français

English descriptors

Abstract

BACKGROUND

Clinical practice for rehabilitation after mild traumatic brain injury (mTBI) is variable, and guidance on when to initiate physical therapy is lacking. Wearable sensor technology may aid clinical assessment, performance monitoring, and exercise adherence, potentially improving rehabilitation outcomes during unsupervised home exercise programs.

OBJECTIVE

The objectives of this study were to: (1) determine whether initiating rehabilitation earlier than typical will improve outcomes after mTBI, and (2) examine whether using wearable sensors during a home-exercise program will improve outcomes in participants with mTBI.

DESIGN

This was a randomized controlled trial.

SETTING

This study will take place within an academic hospital setting at Oregon Health & Science University and Veterans Affairs Portland Health Care System, and in the home environment.

PARTICIPANTS

This study will include 160 individuals with mTBI.

INTERVENTION

The early intervention group (n = 80) will receive one-on-one physical therapy 8 times over 6 weeks and complete daily home exercises. The standard care group (n = 80) will complete the same intervention after a 6- to 8-week wait period. One-half of each group will receive wearable sensors for therapist monitoring of patient adherence and quality of movements during their home exercise program.

MEASUREMENTS

The primary outcome measure will be the Dizziness Handicap Inventory score. Secondary outcome measures will include symptomatology, static and dynamic postural control, central sensorimotor integration posturography, and vestibular-ocular-motor function.

LIMITATIONS

Potential limitations include variable onset of care, a wide range of ages, possible low adherence and/or withdrawal from the study in the standard of care group, and low Dizziness Handicap Inventory scores effecting ceiling for change after rehabilitation.

CONCLUSIONS

If initiating rehabilitation earlier improves primary and secondary outcomes post-mTBI, this could help shape current clinical care guidelines for rehabilitation. Additionally, using wearable sensors to monitor performance and adherence may improve home exercise outcomes.


DOI: 10.1093/ptj/pzaa007
PubMed: 31951263


Affiliations:


Links toward previous steps (curation, corpus...)


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<term>Adult (MeSH)</term>
<term>Ambulatory Care (methods)</term>
<term>Brain Concussion (rehabilitation)</term>
<term>Exercise Therapy (methods)</term>
<term>Home Care Services (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Outcome Assessment, Health Care (MeSH)</term>
<term>Randomized Controlled Trials as Topic (MeSH)</term>
<term>Sample Size (MeSH)</term>
<term>Time Factors (MeSH)</term>
<term>Treatment Outcome (MeSH)</term>
<term>Wearable Electronic Devices (MeSH)</term>
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<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Commotion de l'encéphale (rééducation et réadaptation)</term>
<term>Dispositifs électroniques portables (MeSH)</term>
<term>Essais contrôlés randomisés comme sujet (MeSH)</term>
<term>Facteurs temps (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Services de soins à domicile (MeSH)</term>
<term>Soins ambulatoires (méthodes)</term>
<term>Taille de l'échantillon (MeSH)</term>
<term>Traitement par les exercices physiques (méthodes)</term>
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<term>Ambulatory Care</term>
<term>Exercise Therapy</term>
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<term>Soins ambulatoires</term>
<term>Traitement par les exercices physiques</term>
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<term>Brain Concussion</term>
</keywords>
<keywords scheme="MESH" qualifier="rééducation et réadaptation" xml:lang="fr">
<term>Commotion de l'encéphale</term>
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<term>Middle Aged</term>
<term>Outcome Assessment, Health Care</term>
<term>Randomized Controlled Trials as Topic</term>
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<term>Time Factors</term>
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<term>Adulte d'âge moyen</term>
<term>Dispositifs électroniques portables</term>
<term>Essais contrôlés randomisés comme sujet</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>Résultat thérapeutique</term>
<term>Services de soins à domicile</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Clinical practice for rehabilitation after mild traumatic brain injury (mTBI) is variable, and guidance on when to initiate physical therapy is lacking. Wearable sensor technology may aid clinical assessment, performance monitoring, and exercise adherence, potentially improving rehabilitation outcomes during unsupervised home exercise programs.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVE</b>
</p>
<p>The objectives of this study were to: (1) determine whether initiating rehabilitation earlier than typical will improve outcomes after mTBI, and (2) examine whether using wearable sensors during a home-exercise program will improve outcomes in participants with mTBI.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>DESIGN</b>
</p>
<p>This was a randomized controlled trial.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>SETTING</b>
</p>
<p>This study will take place within an academic hospital setting at Oregon Health & Science University and Veterans Affairs Portland Health Care System, and in the home environment.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>PARTICIPANTS</b>
</p>
<p>This study will include 160 individuals with mTBI.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>INTERVENTION</b>
</p>
<p>The early intervention group (n = 80) will receive one-on-one physical therapy 8 times over 6 weeks and complete daily home exercises. The standard care group (n = 80) will complete the same intervention after a 6- to 8-week wait period. One-half of each group will receive wearable sensors for therapist monitoring of patient adherence and quality of movements during their home exercise program.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>MEASUREMENTS</b>
</p>
<p>The primary outcome measure will be the Dizziness Handicap Inventory score. Secondary outcome measures will include symptomatology, static and dynamic postural control, central sensorimotor integration posturography, and vestibular-ocular-motor function.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>LIMITATIONS</b>
</p>
<p>Potential limitations include variable onset of care, a wide range of ages, possible low adherence and/or withdrawal from the study in the standard of care group, and low Dizziness Handicap Inventory scores effecting ceiling for change after rehabilitation.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>If initiating rehabilitation earlier improves primary and secondary outcomes post-mTBI, this could help shape current clinical care guidelines for rehabilitation. Additionally, using wearable sensors to monitor performance and adherence may improve home exercise outcomes.</p>
</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">31951263</PMID>
<DateCompleted>
<Year>2020</Year>
<Month>07</Month>
<Day>03</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>07</Month>
<Day>03</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Electronic">1538-6724</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>100</Volume>
<Issue>4</Issue>
<PubDate>
<Year>2020</Year>
<Month>04</Month>
<Day>17</Day>
</PubDate>
</JournalIssue>
<Title>Physical therapy</Title>
<ISOAbbreviation>Phys Ther</ISOAbbreviation>
</Journal>
<ArticleTitle>The Sensor Technology and Rehabilitative Timing (START) Protocol: A Randomized Controlled Trial for the Rehabilitation of Mild Traumatic Brain Injury.</ArticleTitle>
<Pagination>
<MedlinePgn>687-697</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/ptj/pzaa007</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND">Clinical practice for rehabilitation after mild traumatic brain injury (mTBI) is variable, and guidance on when to initiate physical therapy is lacking. Wearable sensor technology may aid clinical assessment, performance monitoring, and exercise adherence, potentially improving rehabilitation outcomes during unsupervised home exercise programs.</AbstractText>
<AbstractText Label="OBJECTIVE">The objectives of this study were to: (1) determine whether initiating rehabilitation earlier than typical will improve outcomes after mTBI, and (2) examine whether using wearable sensors during a home-exercise program will improve outcomes in participants with mTBI.</AbstractText>
<AbstractText Label="DESIGN">This was a randomized controlled trial.</AbstractText>
<AbstractText Label="SETTING">This study will take place within an academic hospital setting at Oregon Health & Science University and Veterans Affairs Portland Health Care System, and in the home environment.</AbstractText>
<AbstractText Label="PARTICIPANTS">This study will include 160 individuals with mTBI.</AbstractText>
<AbstractText Label="INTERVENTION">The early intervention group (n = 80) will receive one-on-one physical therapy 8 times over 6 weeks and complete daily home exercises. The standard care group (n = 80) will complete the same intervention after a 6- to 8-week wait period. One-half of each group will receive wearable sensors for therapist monitoring of patient adherence and quality of movements during their home exercise program.</AbstractText>
<AbstractText Label="MEASUREMENTS">The primary outcome measure will be the Dizziness Handicap Inventory score. Secondary outcome measures will include symptomatology, static and dynamic postural control, central sensorimotor integration posturography, and vestibular-ocular-motor function.</AbstractText>
<AbstractText Label="LIMITATIONS">Potential limitations include variable onset of care, a wide range of ages, possible low adherence and/or withdrawal from the study in the standard of care group, and low Dizziness Handicap Inventory scores effecting ceiling for change after rehabilitation.</AbstractText>
<AbstractText Label="CONCLUSIONS">If initiating rehabilitation earlier improves primary and secondary outcomes post-mTBI, this could help shape current clinical care guidelines for rehabilitation. Additionally, using wearable sensors to monitor performance and adherence may improve home exercise outcomes.</AbstractText>
<CopyrightInformation>© 2020 American Physical Therapy Association.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Parrington</LastName>
<ForeName>Lucy</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University, Portland, Oregon; and Veterans Affairs Portland Health Care System, Portland, Oregon.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Jehu</LastName>
<ForeName>Deborah A</ForeName>
<Initials>DA</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University; Djavad Mowafaghian Centre for Brain Health, Centre for Hip Health and Mobility, and Department of Physical Therapy, University of British Columbia, Vancouver, British Columbia, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fino</LastName>
<ForeName>Peter C</ForeName>
<Initials>PC</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University; Veterans Affairs Portland Health Care System; and Department of Health, Kinesiology, and Recreation, University of Utah, Salt Lake City, Utah.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Stuart</LastName>
<ForeName>Samuel</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University; and Department of Sport, Exercise and Rehabilitation, Northumbria University, Newcastle upon Tyne, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wilhelm</LastName>
<ForeName>Jennifer</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pettigrew</LastName>
<ForeName>Natalie</ForeName>
<Initials>N</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Murchison</LastName>
<ForeName>Charles F</ForeName>
<Initials>CF</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University; and Department of Biostatistics at the University of Alabama, Birmingham, Alabama.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>El-Gohary</LastName>
<ForeName>Mahmoud</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>ADPM Inc, Portland, Oregon.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>VanDerwalker</LastName>
<ForeName>Jess</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>ADPM Inc.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pearson</LastName>
<ForeName>Sean</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>ADPM Inc.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hullar</LastName>
<ForeName>Timothy</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Department of Otolaryngology-Head and Neck Surgery, Oregon Health & Science University.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chesnutt</LastName>
<ForeName>James C</ForeName>
<Initials>JC</Initials>
<AffiliationInfo>
<Affiliation>Departments of Family Medicine, Neurology, and Orthopedics & Rehabilitation, Oregon Health & Science University.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Peterka</LastName>
<ForeName>Robert J</ForeName>
<Initials>RJ</Initials>
<AffiliationInfo>
<Affiliation>National Center for Rehabilitative Auditory Research, Veterans Affairs Portland Health Care System.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Horak</LastName>
<ForeName>Fay B</ForeName>
<Initials>FB</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University; Veterans Affairs Portland Health Care System; and APDM Inc.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>King</LastName>
<ForeName>Laurie A</ForeName>
<Initials>LA</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurology, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, Portland, OR 97239 (USA); Veterans Affairs Portland Health Care System; and National Center for Rehabilitative Auditory Research, Veterans Affairs Portland Health Care System.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<DataBankList CompleteYN="Y">
<DataBank>
<DataBankName>ClinicalTrials.gov</DataBankName>
<AccessionNumberList>
<AccessionNumber>NCT03479541</AccessionNumber>
</AccessionNumberList>
</DataBank>
</DataBankList>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>T32 DK091317</GrantID>
<Acronym>DK</Acronym>
<Agency>NIDDK NIH HHS</Agency>
<Country>United States</Country>
</Grant>
</GrantList>
<PublicationTypeList>
<PublicationType UI="D000078325">Clinical Trial Protocol</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>Phys Ther</MedlineTA>
<NlmUniqueID>0022623</NlmUniqueID>
<ISSNLinking>0031-9023</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>AIM</CitationSubset>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000553" MajorTopicYN="N">Ambulatory Care</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D001924" MajorTopicYN="N">Brain Concussion</DescriptorName>
<QualifierName UI="Q000534" MajorTopicYN="Y">rehabilitation</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005081" MajorTopicYN="N">Exercise Therapy</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006699" MajorTopicYN="Y">Home Care Services</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017063" MajorTopicYN="N">Outcome Assessment, Health Care</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016032" MajorTopicYN="Y">Randomized Controlled Trials as Topic</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018401" MajorTopicYN="N">Sample Size</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016896" MajorTopicYN="N">Treatment Outcome</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000076251" MajorTopicYN="Y">Wearable Electronic Devices</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2020</Year>
<Month>01</Month>
<Day>17</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2018</Year>
<Month>11</Month>
<Day>16</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2019</Year>
<Month>10</Month>
<Day>04</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>1</Month>
<Day>18</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<Month>1</Month>
<Day>18</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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</History>
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<list>
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<li>Canada</li>
<li>Royaume-Uni</li>
<li>États-Unis</li>
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<li>Alabama</li>
<li>Oregon</li>
<li>Utah</li>
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<name sortKey="Hullar, Timothy" sort="Hullar, Timothy" uniqKey="Hullar T" first="Timothy" last="Hullar">Timothy Hullar</name>
<name sortKey="King, Laurie A" sort="King, Laurie A" uniqKey="King L" first="Laurie A" last="King">Laurie A. King</name>
<name sortKey="Murchison, Charles F" sort="Murchison, Charles F" uniqKey="Murchison C" first="Charles F" last="Murchison">Charles F. Murchison</name>
<name sortKey="Pettigrew, Natalie" sort="Pettigrew, Natalie" uniqKey="Pettigrew N" first="Natalie" last="Pettigrew">Natalie Pettigrew</name>
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</noRegion>
</country>
</tree>
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