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When a test is more than just a test: Findings from patient interviews and survey in the trial of a technology to measure antidepressant medication response (the PReDicT Trial).
Brown, Susan; Ploeger, Cornelia; Guo, Boliang; Petersen, Juliana J; Beckenstrom, Amy C; Browning, Michael; Dawson, Gerard R; Deckert, Jürgen; Dias, Rebecca; Dourish, Colin T; Gorwood, Philip; Kingslake, Jonathan; Menke, Andreas; Sola, Victor Perez; Reif, Andreas; Ruhe, Henricus; Simon, Judit; Stäblein, Michael; van Schaik, Anneke; Veltman, Dick J; Morriss, Richard.
Affiliation
  • Brown S; NIHR MindTech Med Tech Co-operative, University of Nottingham, Nottingham, UK. Electronic address: sue.brown@nottingham.ac.uk.
  • Ploeger C; Institute of General Practice, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Guo B; NIHR ARC East Midlands, University of Nottingham, Nottingham, UK.
  • Petersen JJ; Institute of General Practice, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Beckenstrom AC; P1vital Products Limited, Howbery Park, Wallingford, UK.
  • Browning M; P1vital Products Limited, Howbery Park, Wallingford, UK; P1vital Limited, Howbery Park, Wallingford, UK; Department of Psychiatry, University of Oxford, Oxford, UK; Oxford Health NHS Trust, Oxford, UK.
  • Dawson GR; P1vital Products Limited, Howbery Park, Wallingford, UK; P1vital Limited, Howbery Park, Wallingford, UK.
  • Deckert J; Department of Psychiatry, Psychosomatics and Psychotherapy, Center of Mental Health, University Hospital of Würzburg, Würzburg, Germany.
  • Dias R; P1vital Products Limited, Howbery Park, Wallingford, UK.
  • Dourish CT; P1vital Products Limited, Howbery Park, Wallingford, UK; P1vital Limited, Howbery Park, Wallingford, UK.
  • Gorwood P; Université Paris Cité, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Paris, France; GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, Paris, France.
  • Kingslake J; P1vital Products Limited, Howbery Park, Wallingford, UK; P1vital Limited, Howbery Park, Wallingford, UK.
  • Menke A; Medical Park Chiemseeblick, Department of Psychosomatic Medicine and Psychotherapy, Rasthausstr. 25, 83233 Bernau am Chiemsee, Germany; Department of Psychiatry and Psychotherapy, University Hospital, Ludwig Maximilian University of Munich, Nussbaumstr. 7, 80336 Munich, Germany.
  • Sola VP; Hospital del Mar Medical Research Institute, IMIM, Barcelona, Spain; Centro de Investigación Biomédica en Red (CIBERSAM), Madrid, Spain.
  • Reif A; Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt - Goethe University, Frankfurt am Main, Germany; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.
  • Ruhe H; Department of Psychiatry, Radboudumc, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, the Netherlands.
  • Simon J; Department of Psychiatry, University of Oxford, Oxford, UK; Department of Health Economics, Center for Public Health, Medical University of Vienna, Vienna, Austria.
  • Stäblein M; Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt - Goethe University, Frankfurt am Main, Germany.
  • van Schaik A; Department of Psychiatry, Amsterdam Public Health Research Institute, Amsterdam UMC, Amsterdam, the Netherlands.
  • Veltman DJ; Department of Psychiatry, Amsterdam UMC, Amsterdam Neuroscience, Amsterdam, the Netherlands.
  • Morriss R; NIHR MindTech Med Tech Co-operative, University of Nottingham, Nottingham, UK; NIHR ARC East Midlands, University of Nottingham, Nottingham, UK.
Compr Psychiatry ; 132: 152467, 2024 07.
Article in En | MEDLINE | ID: mdl-38608615
ABSTRACT

BACKGROUND:

A RCT of a novel intervention to detect antidepressant medication response (the PReDicT Test) took place in five European countries, accompanied by a nested study of its acceptability and implementation presented here. The RCT results indicated no effect of the intervention on depression at 8 weeks (primary outcome), although effects on anxiety at 8 weeks and functioning at 24 weeks were found.

METHODS:

The nested study used mixed methods. The aim was to explore patient experiences of the Test including acceptability and implementation, to inform its use within care. A bespoke survey was completed by trial participants in five countries (n = 778) at week 8. Semi-structured interviews were carried out in two countries soon after week 8 (UK n = 22, Germany n = 20). Quantitative data was analysed descriptively; for qualitative data, thematic analysis was carried out using a framework approach. Results of the two datasets were interrogated together.

OUTCOMES:

Survey results showed the intervention was well received, with a majority of participants indicating they would use it again, and it gave them helpful extra information; a small minority indicated the Test made them feel worse. Qualitative data showed the Test had unexpected properties, including instigating a process of reflection, giving participants feedback on progress and new understanding about their illness, and making participants feel supported and more engaged in treatment.

INTERPRETATION:

The qualitative and quantitative results are generally consistent. The Test's unexpected properties may explain why the RCT showed little effect, as properties were experienced across both trial arms. Beyond the RCT, the qualitative data sheds light on measurement reactivity, i.e., how measurements of depression can impact patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antidepressive Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Compr Psychiatry Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antidepressive Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Compr Psychiatry Year: 2024 Type: Article