1
40
8
-
Dublin Core
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Title
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October 2022 List
Text
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October 2022 List
URL Address
<a href="http://doi.org/10.1017/S1478951522000797">http://doi.org/10.1017/S1478951522000797</a>
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Title
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The Neonatal Palliative Care Attitude Scale: Psychometric properties for Portuguese neonatal nurses
Publisher
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Palliative and Supportive Care
Date
A point or period of time associated with an event in the lifecycle of the resource
2022
Subject
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End-of-life; neonatal; nursing; newborn; Neonatal; reliability; validity; education; nurse; palliative; Palliative; of; human; article; female; male; face; software; therapy; scale; validation; error; care; attitude; clinical; controlled; intensive; major; study; unit; factor; alpha; analysis; coefficient; confirmatory; consistency; convergent; Cronbach; degree; discriminant; experiment; Factor; freedom; internal; mean; quantitative; root; squared; supportive; terminal; Validation
Creator
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Sousa F P; Roldao MG; Rebotim AM; Figueira AR; Barbosa J; Fradique E; Santos Curado MA
Description
An account of the resource
BACKGROUND: This study is aimed to perform the translation and cultural adaptation of the Neonatal Palliative Care Attitude Scale (NiPCAS) and evaluation of its psychometric properties with Portuguese neonatal nurses. METHOD(S): The research started with a scoping review that allowed the identification of the NiPCAS. It was a methodological study with a quantitative approach. The semantic equivalence of the items was adjusted with the participation of 20 neonatal nurse experts. They performed facial and quantitative content validation. Psychometric validation of the NiPCAS was performed on a nonprobability nurses sample (n = 283) in 13 level 3 neonatal units between July 2021 and February 2022. Confirmatory factor analysis using the polychoric correlation matrix was performed to estimate factor validity using the "lavaan" package for R statistical software. Internal consistency was estimated using Cronbach's alpha coefficient, and item sensitivity was assessed using the asymmetry and kurtosis coefficients. Empirical indices were considered: chi-square over degrees of freedom; comparative fit index; normed fit index; Tucker-Lewis index, and root mean square error of approximation; average extracted variance and composite reliability were used to assess convergent validity. RESULT(S): Asymmetry and kurtosis were < 3 and < 7 , respectively, suggesting psychometric sensitivity. The convergent validity of the factors was: F1, FCF1 = 0.90 and for F2, FCF2 = 0.80, and a lower value for F3, FCF3 = 0.40. According to the squared correlation criterion average variance extracted (AVE) between the factors, there was no discriminant validity for F1 and F2, but there was discriminant validity for F1, F3, F2, and F3. SIGNIFICANCE OF RESULTS: This instrument has implications for providing end-of-life care to newborns and their families. The use of this instrument reveals several barriers and facilitating elements inherent in the organization and culture of the facility and nursing education.
Identifier
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<a href="http://doi.org/10.1017/S1478951522000797">10.1017/S1478951522000797</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2022
alpha
Analysis
Article
Attitude
Barbosa J
CARE
Clinical
coefficient
confirmatory
consistency
controlled
convergent
Cronbach
degree
discriminant
Education
end-of-life
error
experiment
Face
factor
Female
Figueira AR
Fradique E
Freedom
Human
intensive
internal
Major
Male
mean
Neonatal
Newborn
Nurse
Nursing
October 2022 List
Of
Palliative
Palliative & Supportive Care
quantitative
Rebotim AM
Reliability
Roldao MG
root
Santos Curado MA
Scale
Software
Sousa F P
squared
study
supportive
terminal
Therapy
Unit
VALIDATION
Validity
-
Dublin Core
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Title
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December 2021 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
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December 2021 List
URL Address
<a href="http://doi.org/10.3390/children8100905" target="_blank" rel="noreferrer noopener">http://doi.org/10.3390/children8100905</a>
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Title
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Validation of the FACETS-OF-PPC as an Outcome Measure for Children with Severe Neurological Impairment and Their Families-A Multicenter Prospective Longitudinal Study
Publisher
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Children
Date
A point or period of time associated with an event in the lifecycle of the resource
2021
Subject
The topic of the resource
pediatric; prospective study; palliative care; multicenter study; validation; factor analysis; patient-centered outcome measures
Creator
An entity primarily responsible for making the resource
Pelke S; Wager J; Claus BB; Stening K; Zernikow B; Reuther M
Description
An account of the resource
Outcome measurement in pediatric palliative care (PPC) is receiving increasing attention. The FACETS-OF-PPC, a multidimensional outcome measure for children with severe neurological impairment, has been developed and partly validated. This study aimed to conclude the validity of the German version of the FACETS-OF-PPC. A multicenter prospective study with two points of measurement has been conducted, employing confirmatory factor analyses, reliability analyses, and analyses to evaluate the tool's sensitivity to change. Overall, 25 inpatient and outpatient teams throughout Germany recruited N = 227 parents of affected children and N = 238 professional caregivers. Participants filled out the FACETS-OF-PPC on the admission of a child to a palliative care service and at discharge from inpatient settings or two months after admission to outpatient services. The analyses revealed the questionnaire needing further adaption. Now, 17 of the original 34 items contribute to the construction of the questionnaire scales. The other items remain part of the questionnaire and may be evaluated descriptively. Furthermore, the FACETS-OF-PPC has moderate to appropriate internal consistency and is sensitive to change. Creating an outcome measure with good psychometric properties for the vulnerable population of children with severe neurological impairment appears extremely difficult. Considering these challenges, the FACETS-OF-PPC demonstrates adequate psychometric properties.
Identifier
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<a href="http://doi.org/10.3390/children8100905" target="_blank" rel="noreferrer noopener">10.3390/children8100905</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2021
Children
Claus BB
December 2021 List
Factor Analysis
Multicenter Study
Palliative Care
patient-centered outcome measures
Pediatric
Pelke S
Prospective Study
Reuther M
Stening K
VALIDATION
Wager J
Zernikow B
-
Dublin Core
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Title
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September 2020 List
Text
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Citation List Month
September 2020 List
URL Address
<a href="http://doi.org/10.1089/jpm.2020.0148" target="_blank" rel="noreferrer noopener">http://doi.org/10.1089/jpm.2020.0148</a>
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Title
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A Tool for the Evaluation of Clinical Needs and Eligibility to Pediatric Palliative Care: The Validation of the ACCAPED Scale
Publisher
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Journal of palliative medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2020
Subject
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assessment; clinical needs; palliative pediatric care; pediatric palliative care; validation
Creator
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Lazzarin P; Giacomelli L; Terrenato I; Benini F
Description
An account of the resource
Background: Despite their importance, pediatric palliative care (PPC) services are still scantly diffused. In addition, eligibility criteria for PPC are quite complex. Consequently, clinicians require a tool that suggests how to refer patients with life-limiting diseases to the most appropriate service and how to properly allocate health care resources. Objective(s): Recently, the Accertamento dei bisogni Clinico-Assistenziali Complessi in PEDiatria (ACCAPED) scale has been developed by a group of experts in PPC to evaluate the specific clinical needs of pediatric patients with a life-limiting disease. This study presents the validation of the ACCAPED scale. Design(s): Validation of ACCAPED scale was pursued by means of description and analysis of clinical vignettes representing patients with challenging-to-evaluate needs who have to be referred to the most appropriate service (community care, general PPC, and specialized PPC). The evaluation of vignettes according to the clinical experience of the experts represented the gold standard against which the validity of the ACCAPED scale was tested by groups with different levels of experience (experts, pediatricians, and health care providers (HCPs) not involved in PPC). Result(s): Results show a very high concordance between the evaluation of the vignettes through the ACCAPED scale and the evaluation by the clinical experience for experts in PPC and pediatricians. A less favorable grade of concordance has been recorded for HCPs not involved in PPC, suggesting that educational efforts to improve basic knowledge of PPC within the medical community are needed. Conclusion(s): Overall, this study suggests that the ACCAPED scale is a useful tool to improve rationalization of resources and eligibility criteria for PPC.
Identifier
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<a href="http://doi.org/10.1089/jpm.2020.0148" target="_blank" rel="noreferrer noopener">10.1089/jpm.2020.0148</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2020
Assessment
Benini F
clinical needs
Giacomelli L
Journal of Palliative Medicine
Lazzarin P
palliative pediatric care
Pediatric Palliative Care
September 2020 List
Terrenato I
VALIDATION
-
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Title
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Treatment of Symptoms in Children with Q3 Conditions Scoping Review Results
Text
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URL Address
<a href="http://doi.org/10.1007/s10545-011-9388-3" target="_blank" rel="noreferrer noopener">http://doi.org/10.1007/s10545-011-9388-3</a>
Dublin Core
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Title
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The quick motor function test: a new tool to rate clinical severity and motor function in Pompe patients
Publisher
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Journal of Inherited Metabolic Disease
Date
A point or period of time associated with an event in the lifecycle of the resource
2012
Subject
The topic of the resource
children; responsiveness; Medicine; Endocrinology & Metabolism; Genetics & Heredity; Research & Experimental; disease; scale; acid maltase deficiency; genotype-phenotype correlation; muscle function; muscular-dystrophy; natural course; validation; tone and motor problems; glycogen storage disease type II; tool development; scale development; motor function
Creator
An entity primarily responsible for making the resource
van Capelle C I; van der Beek N A M E; de Vries J M; van Doorn P A; Duivenvoorden H J; Leshner R T; Hagemans M L C; van der Ploeg A T
Description
An account of the resource
Pompe disease is a lysosomal storage disorder characterized by progressive muscle weakness. With the emergence of new treatment options, psychometrically robust outcome measures are needed to monitor patients' clinical status. We constructed a motor function test that is easy and quick to use. The Quick Motor Function Test (QMFT) was constructed on the basis of the clinical expertise of several physicians involved in the care of Pompe patients; the Gross Motor Function Measure and the IPA/Erasmus MC Pompe survey. The test comprises 16 items. Validity and test reliability were determined in a cohort of 91 Pompe patients (5 to 76 years of age). In addition, responsiveness of the scale to changes in clinical condition over time was examined in a subgroup of 18 patients receiving treatment and 23 untreated patients. Interrater and intrarater reliabilities were good (intraclass correlation coefficients: 0.78 to 0.98 and 0.76 to 0.98). The test correlated strongly with proximal muscle strength assessed by hand held dynamometry and manual muscle testing (rs= 0.81, rs=0.89), and showed significant differences between patient groups with different disease severities. A clinical-empirical exploration to assess responsiveness showed promising results, albeit it should be repeated in a larger group of patients. In conclusion, the Quick Motor Function Test can reliably rate clinical severity and motor function in children and adults with Pompe disease.
Identifier
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<a href="http://doi.org/10.1007/s10545-011-9388-3" target="_blank" rel="noreferrer noopener">10.1007/s10545-011-9388-3</a>
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2012
acid maltase deficiency
Children
de Vries J M
Disease
Duivenvoorden H J
Endocrinology & Metabolism
Genetics & Heredity
genotype-phenotype correlation
glycogen storage disease type II
Hagemans M L C
Journal Of Inherited Metabolic Disease
Leshner R T
Medicine
motor function
muscle function
muscular-dystrophy
natural course
Research & Experimental
responsiveness
Scale
scale development
tone and motor problems
tool development
VALIDATION
van Capelle C I
van der Beek N A M E
van der Ploeg A T
van Doorn P A
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Treatment of Symptoms in Children with Q3 Conditions Scoping Review Results
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1016/j.sleep.2013.09.019" target="_blank" rel="noreferrer noopener">http://doi.org/10.1016/j.sleep.2013.09.019</a>
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Title
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The development and psychometric assessment of a questionnaire to assess sleep and daily troubles in parents of children and young adults with severe psychomotor impairment
Publisher
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Sleep Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2014
Subject
The topic of the resource
caregivers; Validity; Screening; disability; behavior; Neurosciences & Neurology; disturbances; cerebral-palsy; test-retest reliability; instrument; validation; Children with severe psychomotor; HOST; impairment; maternal sleep; Parents' impairment; Parents' questionnaire; quality index; Sleep disturbances; sleep disturbance/disorders; unclear Q3 conditions; Q3 conditions; trajectory; characteristics; tool development; scale development
Creator
An entity primarily responsible for making the resource
Tietze A L; Zernikow B; Otto M; Hirschfeld G; Michel E; Koh M; Blankenburg M
Description
An account of the resource
Background: Children with severe psychomotor impairment (SPMI) often experience sleep disturbances that severely distress both the child and his or her parents. Validated questionnaires for the assessment of parents' distress related to their child's sleep disturbances are lacking. Methods: We developed and validated a new questionnaire, the HOST (holistic assessment of sleep and daily troubles in parents of children with SPMI) to assess the effect of the sleep disturbances in children with SPMI on their parents. The questionnaire was developed based on published data and expert opinion, and it was refined via direct consultation with affected parents. Its psychometric characteristics were assessed in a sample of parents of 214 children with SPMI. It was retested using a random subsample of the participants. Results: Explorative factor analysis revealed that the HOST was composed of four scales. Fit indices, item analysis, and convergent validity (coherence with preexisting instruments of sleep disturbances and health status) were adequate. Retest analysis (n = 62) revealed high stability of the HOST questionnaire and adequate replication validity. Conclusion: Sleep-related difficulties significantly impact the sociomedical characteristics of the parents of children with complex neurologic diseases. Typically, parents are severely affected in various aspects of daily life (i.e., medical health, social life, professional life). The HOST proved to be a valid, reliable and economical assessment tool of sleep-related difficulties in parents and relatives of children with SPMI. The HOST is capable of identifying individuals and specific areas requiring intervention. (C) 2013 Elsevier B.V. All rights reserved.
Identifier
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<a href="http://doi.org/10.1016/j.sleep.2013.09.019" target="_blank" rel="noreferrer noopener">10.1016/j.sleep.2013.09.019</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2014
Behavior
Blankenburg M
Caregivers
cerebral-palsy
characteristics
Children with severe psychomotor
Disability
disturbances
Hirschfeld G
HOST
impairment
instrument
Koh M
maternal sleep
Michel E
Neurosciences & Neurology
Otto M
Parents' impairment
Parents' questionnaire
Q3 conditions
quality index
scale development
Screening
sleep disturbance/disorders
Sleep disturbances
Sleep Medicine
test-retest reliability
Tietze A L
tool development
Trajectory
unclear Q3 conditions
VALIDATION
Validity
Zernikow B
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Treatment of Symptoms in Children with Q3 Conditions Scoping Review Results
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1111/j.1365-2788.2011.01506.x" target="_blank" rel="noreferrer noopener">http://doi.org/10.1111/j.1365-2788.2011.01506.x</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
The Behavior Problems Inventory-Short Form for individuals with intellectual disabilities: Part II: reliability and validity
Publisher
An entity responsible for making the resource available
Journal of Intellectual Disability Research
Date
A point or period of time associated with an event in the lifecycle of the resource
2012
Subject
The topic of the resource
children; reliability; Rehabilitation; validity; Neurology; Education & Educational Research; Genetics & Heredity; Neurosciences &; Psychiatry; autism spectrum disorders; developmental-disabilities; checklist; disabilities; validation; Behavior Problems Inventory; diagnostic-assessment; factor structure; fit indexes; handicapped dash; intellectual; profound mental-retardation; rating form; severely; behavioral problems; unspecified ID; tool development; scale development
Creator
An entity primarily responsible for making the resource
Rojahn J; Rowe E W; Sharber A C; Hastings R; Matson J L; Didden R; Kroes D B H; Dumont E L M
Description
An account of the resource
Background The Behavior Problems Inventory-01 (BPI-01) is an informant-based behaviour rating instrument for intellectual disabilities (ID) with 49 items and three sub-scales: Self-injurious Behavior, Stereotyped Behavior and Aggressive/Destructive Behavior. The Behavior Problems Inventory-Short Form (BPI-S) is a BPI-01 spin-off with 30 items. Methods The psychometric properties of these two versions of the scale were computed using aggregated archival data from nine different sites in the USA, Wales, England, the Netherlands and Romania with a total of 1122 cases with a BPI-01 total score >0. Results The internal consistency of the BPI-01 and the BPI-S ranged from fair to excellent with the BPI-01 showing slightly stronger reliability. Construct validity (confirmatory and discriminant) was computed by comparing BPI sub-scale scores with the scores of four other behaviour rating scales (the Aberrant Behavior Checklist, the Diagnostic Assessment for the Severely Handicapped-II, the Nisonger Child Behavior Rating Form and the Inventory for Client and Agency Planning). Strong evidence for confirmatory and discriminant validity was found for both the BPI-01 and the BPI-S. Confirmatory fit indices for the BPI and the BPI-S were comparable and suggesting that the factor structures fit the data well. Conclusion In summary, both BPI versions were found to be equally sound psychometrically and can be endorsed for future use. However, independent future studies are needed to replicate the psychometrics of the BPI-S with new data.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/j.1365-2788.2011.01506.x" target="_blank" rel="noreferrer noopener">10.1111/j.1365-2788.2011.01506.x</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2012
autism spectrum disorders
Behavior Problems Inventory
behavioral problems
Checklist
Children
Developmental-disabilities
diagnostic-assessment
Didden R
Disabilities
Dumont E L M
Education & Educational Research
factor structure
fit indexes
Genetics & Heredity
handicapped dash
Hastings R
intellectual
Journal Of Intellectual Disability Research
Kroes D B H
Matson J L
Neurology
Neurosciences &
profound mental-retardation
Psychiatry
rating form
Rehabilitation
Reliability
Rojahn J
Rowe E W
scale development
severely
Sharber A C
tool development
unspecified ID
VALIDATION
Validity
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Treatment of Symptoms in Children with Q3 Conditions Scoping Review Results
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1016/j.nmd.2014.01.003" target="_blank" rel="noreferrer noopener">http://doi.org/10.1016/j.nmd.2014.01.003</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients
Publisher
An entity responsible for making the resource available
Neuromuscular Disorders
Date
A point or period of time associated with an event in the lifecycle of the resource
2014
Subject
The topic of the resource
responsiveness; Neurosciences & Neurology; Spinal muscular atrophy; trial; spinal muscular-atrophy; validation; neuromuscular diseases; Outcome measures; walk test; tone and motor problems; SMA1; tool development; scale development; HMFS; MFM
Creator
An entity primarily responsible for making the resource
Mazzone E; De Sanctis R; Fanelli L; Bianco F; Main M; van den Hauwe M; Ash M; de Vries R; Mata J F; Schaefer K; D'Amico A; Colia G; Palermo C; Scoto M; Mayhew A; Eagle M; Servais L; Vigo M; Febrer A; Korinthenberg R; Jeukens M; de Viesser M; Totoescu A; Voit T; Bushby K; Muntoni F; Goemans N; Bertini E; Pane M; Mercuri E
Description
An account of the resource
The aim of this prospective longitudinal multi centric study was to evaluate the correlation between the Hammersmith Functional Motor Scale and the 20 item version of the Motor Function Measure in non ambulant SMA children and adults at baseline and over a 12 month period. Seventy-four non-ambulant patients performed both measures at baseline and 49 also had an assessment 12 month later. At baseline the scores ranged between 0 and 40 on the Hammersmith Motor function Scale and between 3 and 45 on the Motor Function Measure 20. The correlation between the two scales was 0.733. The 12 month changes ranged between 11 and 4 for the Hammersmith and between 11 and 7 for the Motor Function Measure 20. The correlation between changes was 0.48. Our results suggest that both scales provide useful information although they appeared to work differently at the two extremes of the spectrum of abilities. The Hammersmith Motor Function Scale appeared to be more suitable in strong non ambulant patients, while the Motor Function Measures appeared to be more sensitive to capture activities and possible changes in the very weak patients, including more items capturing axial and upper limb activities. The choice of these measures in clinical trials should therefore depend on inclusion criteria and magnitude of expected changes. (C) 2014 Published by Elsevier B.V.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.nmd.2014.01.003" target="_blank" rel="noreferrer noopener">10.1016/j.nmd.2014.01.003</a>
Rights
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2014
Ash M
Bertini E
Bianco F
Bushby K
Colia G
D'Amico A
De Sanctis R
de Viesser M
de Vries R
Eagle M
Fanelli L
Febrer A
Goemans N
HMFS
Jeukens M
Korinthenberg R
Main M
Mata J F
Mayhew A
Mazzone E
Mercuri E
MFM
Muntoni F
Neuromuscular Diseases
Neuromuscular Disorders
Neurosciences & Neurology
Outcome measures
Palermo C
Pane M
responsiveness
scale development
Schaefer K
Scoto M
Servais L
SMA1
Spinal Muscular Atrophy
spinal muscular-atrophy
tone and motor problems
tool development
Totoescu A
trial
VALIDATION
van den Hauwe M
Vigo M
Voit T
walk test
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.pec.2011.01.009" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.pec.2011.01.009</a>
<a href="http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000298219800009" target="_blank" rel="noreferrer">http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000298219800009</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Perception of empathy in the therapeutic encounter: Effects on the common cold
Publisher
An entity responsible for making the resource available
Patient Education And Counseling
Date
A point or period of time associated with an event in the lifecycle of the resource
2011
Subject
The topic of the resource
empathy; Health aspects; family medicine; CARE MEASURE; Common Cold - therapy; health outcomes; PLACEBO; CARE; Cold (Disease); Common cold; Common Cold - psychology; CONTEXT; CONTROLLED-TRIAL; ECHINACEA; ENVIRONMENTAL & OCCUPATIONAL HEALTH; EXPECTATIONS; GENERAL-PRACTICE CONSULTATIONS; Interdisciplinary; Interleukin-8 - analysis; Medical informatics; Neutrophils - immunology; Patient-practitioner interaction; PUBLIC; RESPIRATORY SYMPTOM SURVEY; SOCIAL SCIENCES; Therapeutic encounter; VALIDATION
Creator
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Rakel D; Barrett B; Zhang ZJ; Hoeft T; Chewning B; Marchand L; Scheder J
Description
An account of the resource
To evaluate the effects of patient-practitioner interaction on the severity and duration of the common cold.
Identifier
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<a href="http://doi.org/10.1016/j.pec.2011.01.009" target="_blank" rel="noreferrer">10.1016/j.pec.2011.01.009</a>
Rights
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2011
Backlog
Barrett B
CARE
CARE MEASURE
Chewning B
Cold (Disease)
Common cold
Common Cold - psychology
Common Cold - therapy
CONTEXT
CONTROLLED-TRIAL
ECHINACEA
Empathy
Environmental & Occupational Health
EXPECTATIONS
family medicine
GENERAL-PRACTICE CONSULTATIONS
Health Aspects
health outcomes
Hoeft T
Interdisciplinary
Interleukin-8 - analysis
Journal Article
Marchand L
Medical informatics
Neutrophils - immunology
Patient Education and Counseling
Patient-practitioner interaction
PLACEBO
Public
Rakel D
RESPIRATORY SYMPTOM SURVEY
Scheder J
Social Sciences
Therapeutic encounter
VALIDATION
Zhang ZJ