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A protocol for a multicentre, parallel-group, pragmatic randomised controlled trial to evaluate the NEVERMIND system in preventing and treating depression in patients with severe somatic conditions.
Carli, Vladimir; Wasserman, Danuta; Hadlaczky, Gergö; Petros, Nuhamin Gebrewold; Carletto, Sara; Citi, Luca; Dinis, Sergio; Gentili, Claudio; Gonzalez-Martinez, Sergio; Meyer, Björn; Ostacoli, Luca; Ottaviano, Manuel; Ouakinin, Silvia; Paradiso, Rita; Poli, Riccardo; Rocha, Isabel; Settanta, Carmen; Waldmeyer, Maria Teresa Arredondo; Valenza, Gaetano; Scilingo, Enzo Pasquale.
Afiliación
  • Carli V; National Centre for Suicide Research and Prevention of Mental Ill-Health, Karolinska Institutet, Stockholm, Sweden. Vladimir.carli@ki.se.
  • Wasserman D; National Centre for Suicide Research and Prevention of Mental Ill-Health, Karolinska Institutet, Stockholm, Sweden.
  • Hadlaczky G; National Centre for Suicide Research and Prevention of Mental Ill-Health, Karolinska Institutet, Stockholm, Sweden.
  • Petros NG; National Centre for Suicide Research and Prevention of Mental Ill-Health, Karolinska Institutet, Stockholm, Sweden.
  • Carletto S; Department of Neuroscience "Rita Levi Montalcini", Università degli Studi di Torino, Turin, Italy.
  • Citi L; School of Computer Science and Electronic Engineering, University of Essex, Colchester, UK.
  • Dinis S; Faculdade de Medicina and CCUL, Universidade de Lisboa, Lisbon, Portugal.
  • Gentili C; General Psychology Department, Università degli Studi di Padova, Padua, Italy.
  • Gonzalez-Martinez S; Life Supporting Technologies, Universidad Politécnica de Madrid, Madrid, Spain.
  • Aldo De Leonibus; Inventya LTD, Daresbury, UK.
  • Meyer B; GAIA AG, Hamburg, Germany.
  • Ostacoli L; Department of Clinical and Biological Sciences, Università degli studi di Torino, Turin, Italy.
  • Ottaviano M; Life Supporting Technologies, Universidad Politécnica de Madrid, Madrid, Spain.
  • Ouakinin S; Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
  • Paradiso R; Smartex, Pisa, Italy.
  • Poli R; School of Computer Science and Electronic Engineering, University of Essex, Colchester, UK.
  • Rocha I; Faculdade de Medicina and CCUL, Universidade de Lisboa, Lisbon, Portugal.
  • Settanta C; Department of Clinical and Biological Sciences, Università degli studi di Torino, Turin, Italy.
  • Waldmeyer MTA; Life Supporting Technologies, Universidad Politécnica de Madrid, Madrid, Spain.
  • Valenza G; Research Center "E.Piaggio" and Department of Information Engineering, School of Engineering, University of Pisa, Pisa, Italy.
  • Scilingo EP; Research Center "E.Piaggio" and Department of Information Engineering, School of Engineering, University of Pisa, Pisa, Italy.
BMC Psychiatry ; 20(1): 93, 2020 03 02.
Article en En | MEDLINE | ID: mdl-32122315
ABSTRACT

BACKGROUND:

Depressive symptoms are common in individuals suffering from severe somatic conditions. There is a lack of interventions and evidence-based interventions aiming to reduce depressive symptoms in patients with severe somatic conditions. The aim of the NEVERMIND project is to address these issues and provide evidence by testing the NEVERMIND system, designed to reduce and prevent depressive symptoms in comparison to treatment as usual.

METHODS:

The NEVERMIND study is a parallel-groups, pragmatic randomised controlled trial to assess the effectiveness of the NEVERMIND system in reducing depressive symptoms among individuals with severe somatic conditions. The NEVERMIND system comprises a smart shirt and a user interface, in the form of a mobile application. The system is a real-time decision support system, aiming to predict the severity and onset of depressive symptoms by modelling the well-being condition of patients based on physiological data, body movement, and the recurrence of social interactions. The study includes 330 patients who have a diagnosis of myocardial infarction, breast cancer, prostate cancer, kidney failure, or lower limb amputation. Participants are randomised in blocks of ten to either the NEVERMIND intervention or treatment as usual as the control group. Clinical interviews and structured questionnaires are administered at baseline, at 12 weeks, and 24 weeks to assess whether the NEVERMIND system is superior to treatment as usual. The endpoint of primary interest is Beck Depression Inventory II (BDI-II) at 12 weeks defined as (i) the severity of depressive symptoms as measured by the BDI-II. Secondary outcomes include prevention of the onset of depressive symptoms, changes in quality of life, perceived stigma, and self-efficacy.

DISCUSSION:

There is a lack of evidence-based interventions aiming to reduce and prevent depressive symptoms in patients with severe somatic conditions. If the NEVERMIND system is effective, it will provide healthcare systems with a novel and innovative method to attend to depressive symptoms in patients with severe somatic conditions. TRIAL REGISTRATION DRKS00013391. Registered 23 November 2017.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Calidad de Vida / Depresión Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research Límite: Humans / Male Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Calidad de Vida / Depresión Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research Límite: Humans / Male Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Suecia