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Prescriptive factors for intensive home treatment in acute psychiatry: a secondary analysis of a randomised controlled trial.
Barakat, Ansam; Blankers, Matthijs; Cornelis, Jurgen E; Lommerse, Nick M; Beekman, Aartjan Tf; Dekker, Jack Jm.
Afiliación
  • Barakat A; Department of Research, Arkin Institute for Mental Health Care, Amsterdam, The Netherlands. ansambraam@gmail.com.
  • Blankers M; Department of Psychiatry Amsterdam UMC/VUmc, Amsterdam Public Health research institute Amsterdam UMC, Amsterdam, The Netherlands. ansambraam@gmail.com.
  • Cornelis JE; Department of Research, Arkin Institute for Mental Health Care, Amsterdam, The Netherlands.
  • Lommerse NM; Trimbos-Institute, Netherlands Institute of Mental Health and Addiction, Utrecht, The Netherlands.
  • Beekman AT; Department of Psychiatry Amsterdam UMC/AMC, Amsterdam Public Health research institute Amsterdam UMC, Amsterdam, The Netherlands.
  • Dekker JJ; Department of Research, Arkin Institute for Mental Health Care, Amsterdam, The Netherlands.
Int J Ment Health Syst ; 18(1): 2, 2024 Jan 03.
Article en En | MEDLINE | ID: mdl-38172935
ABSTRACT

BACKGROUND:

Intensive home treatment (IHT) aims to prevent psychiatric hospitalisation. Although this intervention is well tested, it is still unknown for whom this intervention works best. Therefore, this study aims to explore prescriptive factors that moderate the effect of IHT compared to care as usual (CAU) on symptom severity.

METHODS:

Using data from a randomised controlled trial, 198 participants that experience an exacerbation of acute psychiatric symptoms were included in this secondary analysis. In order to maximise clinical relevance, generally available environmental and clinical baseline factors were included as tentative moderators age, gender, employment status, domestic situation, psychiatric disorders, psychological symptoms, psychosocial functioning, alcohol and other substance use. The outcome variable symptom severity was measured using the Brief Psychiatric Rating Scale (BPRS) and collected at 26 and 52 weeks post-randomisation. Multiple regression analysis was used to examine which participants' characteristics moderate the effect of IHT on the total BPRS score.

RESULTS:

Our results suggest that being employed (B = 0.28, SE = 0.13, 95% CI = 0.03-0.53, p = 0.03) at baseline seems to have a moderation effect, which result in lower symptom severity scores at 26 weeks follow-up for patients who received IHT. This effect was not found at 52 weeks.

CONCLUSIONS:

On the basis of the number of factors tested, there is no evidence for robust outcome moderators of the effect of IHT versus CAU. Our conclusion is therefore that IHT can be offered to a diverse target population with comparable clinical results. TRIAL REGISTRATION This trial is registered (date of registration 2016-11-23) at the international clinical trials registry platform (NTR6151).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 8_alcohol Tipo de estudio: Clinical_trials Idioma: En Revista: Int J Ment Health Syst Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 8_ODS3_consumo_sustancias_psicoactivas Problema de salud: 8_alcohol Tipo de estudio: Clinical_trials Idioma: En Revista: Int J Ment Health Syst Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos
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