Let It Out (LIO) and COVID19: Testing an Online Emotional Disclosure-based Intervention During the COVID19 Pandemic (LIO-C)
Let It Out (LIO) and COVID19: a Randomised Controlled Trial of an Online Emotional Disclosure-based Intervention for Adults During the COVID19 Pandemic
A randomised controlled trial designed to test whether an online expressive writing intervention (LIO-C) can reduce distress for English-speaking adults during the global COVID19 pandemic.
Hypothesis: LIO-C will improve distress (as measured by K10) in adults at 1 week post-intervention compared to a neutral writing control during the COVID19 pandemic.
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Descrizione dettagliata
The world is currently experiencing unprecedented challenges caused by the global coronavirus (COVID19) pandemic. Many countries are enforcing measures to restrict movement of people to reduce the spread of the outbreak, including lock-downs, social distancing and self-isolation. These methods, although necessary to slow the spread of disease, will have negative effects on psychological well-being of large populations. Shortage of health care professionals and measures to restrict interpersonal contact means facilitated psychological interventions will not be feasible for many, at least during the height of the pandemic. There is therefore a need for self-directed psychological interventions that can be practically and quickly implemented online.
Emotional disclosure-based therapies, such as expressive writing (EW), hold potential as low-cost, easy to implement means of support, with minimal requirement for facilitation. In its original format, EW involved writing daily for 15-20 minutes for 3-4 days about a traumatic event. Since its development, it has been adapted in many ways, including writing about positive events and writing about stress from a compassionate stance. There is evidence that such interventions can provide significant psychological and physical benefits in healthy populations and reduce the effects of natural disasters on health and well-being. However, to our knowledge this form of psychological intervention has not been tested during a rapidly evolving crisis or pandemic.
The aim of this study is to test whether an online self-compassion and EW based intervention (LIO-C) can reduce the negative effects of the COVID19 pandemic on health and well-being. The intervention is based on an existing intervention, LIO, that we previously developed for use in advanced disease populations, in collaboration with clinical and health psychologists, and patient and public representatives. For this study, we have adapted the intervention for people living through the current COVID19 pandemic by altering the writing prompts, and translating the intervention to an online hub. As this is an unfacilitated intervention, the instructions involve writing from a compassionate stance to minimise any potential short term negative effects associated with writing about difficult experiences.
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Kent
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London, Kent, Regno Unito, TN14 6DW
- University College London
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Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- English speaking adults over the age of 18
- Able to read and write clearly in English
Exclusion Criteria:
- None
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
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Sperimentale: LIO-C
Participants receive LIO-C writing intervention
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Participants complete three online 20-minute writing sessions in response to prompts asking them to write about their experiences during the COVID19 pandemic from a self-compassionate perspective
Altri nomi:
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Comparatore placebo: Neutral writing control
Participants receive neutral writing control intervention
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Participants complete three online 20-minute writing sessions in response to neutral writing prompts
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Kessler Psychological Distress Scale (K10)
Lasso di tempo: 1 week post-intervention
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10-item self-report distress scale
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1 week post-intervention
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Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Kessler Psychological Distress Scale (K10)
Lasso di tempo: Immediately and 8 weeks post-intervention
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10-item self-report distress scale
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Immediately and 8 weeks post-intervention
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Perceived Stress Scale (PSS-10)
Lasso di tempo: Immediately, 1 week and 8 weeks post-intervention
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Self-report stress scale
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Immediately, 1 week and 8 weeks post-intervention
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Pittsburgh Sleep Quality Index (PSQI)
Lasso di tempo: Immediately, 1 week and 8 weeks post-intervention
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Self-report sleep scale
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Immediately, 1 week and 8 weeks post-intervention
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Self-compassion scale (SCS)
Lasso di tempo: Immediately, 1 week and 8 weeks post-intervention
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Self-report self-compassion scale
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Immediately, 1 week and 8 weeks post-intervention
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UCLA Loneliness Scale (UCLA LS)
Lasso di tempo: Immediately, 1 week and 8 weeks post-intervention
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Self-report loneliness scale
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Immediately, 1 week and 8 weeks post-intervention
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Uptake of existing mental health services (MHS)
Lasso di tempo: Immediately, 1 week and 8 weeks post-intervention
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Self-report measure of MHS usage
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Immediately, 1 week and 8 weeks post-intervention
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Mood and meaning
Lasso di tempo: Immediately after each writing session
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3-item, 7-point, Likert scale measuring how personal and meaningful participants' felt their writing was and their mood
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Immediately after each writing session
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Acceptability
Lasso di tempo: Immediately post-intervention
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Via an online feedback form
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Immediately post-intervention
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Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Investigatore principale: Nuriye Kupeli, Marie Curie Palliative Care Research Department, UCL
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 15281/003
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
Criteri di accesso alla condivisione IPD
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