- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01179841
Intervention for Toddlers at Risk for Autism Spectrum Disorders (ASD)
9. März 2021 aktualisiert von: Rebecca Landa, Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
A Comprehensive Approach to Intervention for Toddlers at Risk for ASD
This research is being done to test the effectiveness of an early intervention model for very young children at high risk for autism spectrum disorders (ASD) and their families.
If children show improvement in this intervention, the investigators hope that the availability of public services of this type will be increased.
Children between 11 months and 21 months old with Autism Spectrum Disorders, or with social and communication delays that indicate high risk for Autism Spectrum Disorders, and their parents may join the study.
Treatment must start prior to the second birthday.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Tatsächlich)
49
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
-
-
Maryland
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Baltimore, Maryland, Vereinigte Staaten, 21211
- Kennedy Krieger Institute
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
11 Monate bis 1 Jahr (Kind)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- Children will be ascertained between 11 months and 21 months of age
- Must be able to enter the study prior to their second birthday
- Must then pass an eligibility assessment to determine whether the child meets criteria for ASD and thus qualifies for the study. This assessment will consist of the Baby ADOS and the Mullen Scales of Early Learning. Children must meet criteria for ASD or autism on the ADOS, score more than one standard deviation below the mean on the Receptive or Expressive Language scale of the MSEL, and have a clinical judgment of ASD to be eligible for enrollment into treatment.
- Parents must agree to participate in the study and commit to having their child participate in the intervention to which they are randomized for 6 months
- The parent (or other primary caregiver, such as grandparent) in the Parent Enrichment/Training condition must agree to attend the training sessions
Exclusion Criteria:
- Fail hearing or vision screening (by pediatrician's office, audiologist, or ophthalmologist)
- Family's first language being other than English (language measures are normed on English speakers, putting non-English speakers at a disadvantage. In addition, the treatment is delivered in English. Children from non-English speaking homes may not make progress, but for reasons other than the efficacy of the intervention.)
- Head injury (because this may cause some of the symptoms, which may not be due to autism and therefore we would not be able to assess the effects of the intervention on autism)
- Identified reason for the autism (e.g., fragile X syndrome, Rett syndrome, Tuberous Sclerosis)
- Inability of the family to attend the playgroup sessions and parent trainings
- Parents whose hearing or vision is not within normal limits after correction (e.g., hearing aid, glasses)
- Parents with developmental delays, language or learning impairments, or a psychiatric diagnosis IF the impairment would interfere with parent training (PI will assess on a case by case basis by talking to the parent)
- Foster children
- Refusal to allow videotaping of the children's assessments or intervention or to allow videotaped footage to be used for teaching purposes.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Playgroup and Parent Training
|
The playgroup will be conducted at our center and focuses on providing an invigorating learning environment in which emerging skills/knowledge are skillfully brought to a higher level of maturity, integrated with existing abilities, and used functionally.
Learning with and through peers, provides the opportunity to address abnormal peer relationships for developmental level.
Providing an enriched environment with toys, structured learning, and opportunities for ongoing engagement we offer the children experiences that they would not otherwise have.
Parent training sessions will focus on strategies aimed at improving child social engagement and communication.
Parent education sessions will focus on topics related to autism, learning styles, interventions, and resources.
The 1-2 hour individual therapeutic sessions with parent training in the home or clinic (1x every week over six months) are based on our own program which is in development.
This program focuses on teaching parents how to encourage social and communication skills in their toddlers and also provides comprehensive information about development.
Sessions will focus on knowledge of autism, current access to services, general knowledge of strategies used to facilitate child development, advocacy, knowledge of how to access services, and coping strategies.
Andere Namen:
In the once-a-week 1 to 2 hour parent training/enrichment, we will ask parents to target specific play and care routines in which they may stimulate their child's development in the ways identified by the therapist.
These stimulation times may be provided by the parents, other family members, friends, volunteers or hired assistants.
Parents will be encouraged to have their child in direct skill-enhancing engagement for 1-2 hour per day.
The therapist will work with the family to identify times during the day that best lend themselves to accomplishing this goal.
Andere Namen:
|
|
Aktiver Komparator: Parent Training
|
The 1-2 hour individual therapeutic sessions with parent training in the home or clinic (1x every week over six months) are based on our own program which is in development.
This program focuses on teaching parents how to encourage social and communication skills in their toddlers and also provides comprehensive information about development.
Sessions will focus on knowledge of autism, current access to services, general knowledge of strategies used to facilitate child development, advocacy, knowledge of how to access services, and coping strategies.
Andere Namen:
In the once-a-week 1 to 2 hour parent training/enrichment, we will ask parents to target specific play and care routines in which they may stimulate their child's development in the ways identified by the therapist.
These stimulation times may be provided by the parents, other family members, friends, volunteers or hired assistants.
Parents will be encouraged to have their child in direct skill-enhancing engagement for 1-2 hour per day.
The therapist will work with the family to identify times during the day that best lend themselves to accomplishing this goal.
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Developmental Level
Zeitfenster: 3 months into treatment, 6 months into treatment, and 6 months after treatment ends
|
Using the Mullen Scales of Early Learning to assess.
|
3 months into treatment, 6 months into treatment, and 6 months after treatment ends
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Communication
Zeitfenster: 3 months after treatment starts
|
Using Communication and Symbolic Behavior Scales to assess.
|
3 months after treatment starts
|
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Communication
Zeitfenster: 6 months into treatment
|
Using Communication and Symbolic Behavior Scales to assess.
|
6 months into treatment
|
|
Communication
Zeitfenster: 6 months after treatment ends
|
Using Communication and Symbolic Behavior Scales to assess.
|
6 months after treatment ends
|
|
Presence and Severity of Autism
Zeitfenster: 3 months after treatment starts
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Using Autism Diagnostic Observation Schedule to assess.
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3 months after treatment starts
|
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Presence and Severity of Autism
Zeitfenster: 6 months into treatment
|
Using Autism Diagnostic Observation Schedule to assess.
|
6 months into treatment
|
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Presence and Severity of Autism
Zeitfenster: 6 months after treatment ends
|
Using Autism Diagnostic Observation Schedule to assess.
|
6 months after treatment ends
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Mitarbeiter
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Allgemeine Veröffentlichungen
- Keen D, Rodger S, Doussin K, Braithwaite M. A pilot study of the effects of a social-pragmatic intervention on the communication and symbolic play of children with autism. Autism. 2007 Jan;11(1):63-71. doi: 10.1177/1362361307070901.
- Solomon R, Necheles J, Ferch C, Bruckman D. Pilot study of a parent training program for young children with autism: the PLAY Project Home Consultation program. Autism. 2007 May;11(3):205-24. doi: 10.1177/1362361307076842.
- Howlin P, Gordon RK, Pasco G, Wade A, Charman T. The effectiveness of Picture Exchange Communication System (PECS) training for teachers of children with autism: a pragmatic, group randomised controlled trial. J Child Psychol Psychiatry. 2007 May;48(5):473-81. doi: 10.1111/j.1469-7610.2006.01707.x.
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Januar 2008
Primärer Abschluss (Tatsächlich)
1. Dezember 2011
Studienabschluss (Tatsächlich)
1. Dezember 2011
Studienanmeldedaten
Zuerst eingereicht
21. Juli 2010
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
10. August 2010
Zuerst gepostet (Schätzen)
11. August 2010
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
10. März 2021
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
9. März 2021
Zuletzt verifiziert
1. März 2021
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- NA_00006553
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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