- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT03301831
Resourcefulness Intervention With Parents of Technology-Dependent Children
27 settembre 2021 aggiornato da: Valerie Toly, University Hospitals Cleveland Medical Center
Intervention Pilot With Parents of Technology-Dependent Children
Technology-dependent children, those who live at home but rely on medical equipment such as mechanical ventilation or feeding tubes, require complex care for their chronic condition.
Parents usually provide a majority of their care and are often overwhelmed by the caregiving demands resulting in deterioration of their own mental and physical health.
The goal of this 2-arm (intervention vs. attention control) RCT is to test a cognitive-behavioral Resourcefulness Training intervention that includes teaching social (help-seeking) and personal (self-help) resourcefulness skills; ongoing access to video vignettes of caregivers of technology-dependent children describing resourcefulness skill application in daily life; 4 weeks of skills' reinforcement using daily journal writing; weekly phone calls for the first 4 weeks; and booster sessions at 2 and 4 months post enrollment.
The intervention is proposed to improve these caregivers' mental and physical health outcomes and family functioning outcomes while they continue to provide vital care for these vulnerable children.
Panoramica dello studio
Stato
Completato
Intervento / Trattamento
Descrizione dettagliata
Technology-dependent children, those who rely on medical equipment such as mechanical ventilation or feeding tubes for daily care at home, are among the sickest and most vulnerable subset of children with complex chronic conditions.
An estimated 600,000 children in the United States are technology dependent and live at home, and are cared for primarily by their parents.
These parents report greater levels of depressive symptoms and stress than other caregiver groups.
In addition, these caregivers report poor psychological and physical health that compromise their caregiving capacity and increase their use of emergency rooms (ER) for their children's care needs.
Despite these adverse consequences, there are no interventions to meet the needs of these caregivers and their children.
Resourcefulness Training, (cognitive-behavioral self-management intervention) has been shown to improve psychological and physical outcomes, mediate the effects of stress, and enhance the care provided to care-recipients.
It will be tested in a randomized trial against an attention-only control arm.
The intervention arm will receive an intervention that includes: a face-to-face session for teaching social (help-seeking) and personal (self-help) resourcefulness skills; ongoing access to video vignettes of caregivers of technology-dependent children describing resourcefulness skill application in daily life; 4 weeks of skills' reinforcement using daily journal writing; weekly phone calls for the first 4 weeks; and booster sessions at 2 and 4 months post enrollment.
The Attention Control arm will receive weekly phone calls for the first 4 weeks and at 2 and 4 months post enrollment plus any usual care.
The aims of the study are to: 1) Determine whether Resourcefulness Training versus Attention Control improves psychological (general mental health, depressive cognitions, depressive symptoms, appraised stress, burden) and physical outcomes (general physical health, chronic stress [hair cortisol]) and family functioning over 6 months in parents of technology-dependent children, after controlling for the parents' race/ethnicity, sex, family income, and children's functional status; and 2) Determine whether changes in psychological and physical outcomes and family functioning are mediated by changes in parents' levels of resourcefulness (personal and social).
Data collection will take place at baseline then 6 weeks, 3 months, and 6 months post-enrollment.
Our study will be the first to test a resourcefulness intervention for this caregiver population and to include male as well as female caregivers.
This intervention is distinctive in that it uses web, telephone, and journal components for reinforcement-not multiple face-to-face visits that can be labor intensive.
If shown to be efficacious, it can be easily replicated with other populations with strong potential for translation into practice.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
93
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
-
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Ohio
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Cleveland, Ohio, Stati Uniti, 44106-5065
- University Hospitals Cleveland Medical Center
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
Sì
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- parent caregiver (biological, adoptive, or foster mother, father, grandmother or grandfather) for a technology-dependent child based on the Office of Technology Assessment (OTA) classification criteria (Group 1, mechanical ventilator; Group 2, intravenous nutrition/medication; Group 3 respiratory or nutritional support)
- at least 18 years of age
- able to speak and understand English due to the availability of the intervention and instruments in English only
- the technology-dependent child must be age 17 years or younger and receive care in the home from his/her parent
Exclusion Criteria:
- Parents of children with a cancer diagnosis will be excluded from participation due to the potentially life-threatening, terminal nature of the illness and grief reactions associated with a cancer diagnosis that may limit their ability to participate over the 6 month study.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Resourcefulness Training Intervention
The intervention arm will receive an intervention that includes: a face-to-face session for teaching social (help-seeking) and personal (self-help) resourcefulness skills; ongoing access to video vignettes of caregivers of technology-dependent children describing resourcefulness skill application in daily life; 4 weeks of skills' reinforcement using daily journal writing; weekly phone calls for the first 4 weeks; and booster sessions at 2 and 4 months post enrollment.
|
Cognitive-behavioral intervention that includes personal and social resourcefulness skills.
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Nessun intervento: Attention Control
The Attention Control arm will receive weekly phone calls for the first 4 weeks and at 2 and 4 months post enrollment plus any usual care.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Depressive Cognitions Scale
Lasso di tempo: From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
Subjective measure of participant depressive cognitions- precursor of depressive symptoms.
Score range for the instrument is 0-40, where a higher score indicates greater depressive cognition.
|
From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
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Medical Outcomes Short Form Health Survey (SF-12) Physical Health
Lasso di tempo: From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
Change in General Mental and Physical Health from Baseline to 6 Months Post Enrollment.
Score range is 0-100, where a '0' indicates lowest level of health, and '100' indicates highest level of health.
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From baseline to 6 weeks, 3 months, and 6 months post-enrollment
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Medical Outcomes Short Form Health Survey (SF-12) Mental Health
Lasso di tempo: From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
Change in General Mental and Physical Health from Baseline to 6 Months Post Enrollment.
Score range is 0-100, where a '0' indicates lowest level of health, and '100' indicates highest level of health.
|
From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Feetham Family Functioning Survey
Lasso di tempo: From baseline to 6 weeks, 3 months, and 6 months post-enrollment
|
Change in Family Functioning from Baseline to 6 Months Post Enrollment.
This subjective measure of family functioning is collected via participant survey.
The score range is 0-175, which is the sum of the "differences" between reality and life expectations.
Higher 'Difference' score indicates an imbalance between reality and life expectations
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From baseline to 6 weeks, 3 months, and 6 months post-enrollment
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Resourcefulness Scale
Lasso di tempo: From baseline to 6 weeks, 3 months, and 6 months post-enrollment
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Subjective survey of participants' personal and social resourcefulness.
Score range is 0-140, where a higher score indicates greater resourcefulness.
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From baseline to 6 weeks, 3 months, and 6 months post-enrollment
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Investigatori
- Investigatore principale: Valerie A Toly, PhD, Frances Payne Bolton School of Nursing, Case Western Reserve University
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
5 febbraio 2018
Completamento primario (Effettivo)
9 dicembre 2019
Completamento dello studio (Effettivo)
9 dicembre 2019
Date di iscrizione allo studio
Primo inviato
24 settembre 2017
Primo inviato che soddisfa i criteri di controllo qualità
28 settembre 2017
Primo Inserito (Effettivo)
4 ottobre 2017
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
25 ottobre 2021
Ultimo aggiornamento inviato che soddisfa i criteri QC
27 settembre 2021
Ultimo verificato
1 settembre 2021
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 08-10-30
- 1R15NR017302-01 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Descrizione del piano IPD
The study team is still conducting analysis and writing up study results for publication.
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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