Remote blended treatment for individuals with suicidal ideation: A single‐arm proof‐of‐concept trial

Author:

Büscher Rebekka1ORCID,Teismann Tobias2ORCID,Hartleitner Paula1,Klein Jan Philipp3,Baumeister Harald4,Sander Lasse B.1

Affiliation:

1. Department of Medical Psychology and Medical Sociology, Faculty of Medicine University of Freiburg Freiburg Germany

2. Mental Health Research and Treatment Center, Department of Psychology Ruhr‐Universität Bochum Germany

3. Department of Psychiatry, Psychosomatics and Psychotherapy Luebeck University Luebeck Germany

4. Department of Clinical Psychology and Psychotherapy, Institute of Psychology and Education Ulm University Ulm Germany

Abstract

AbstractIntroductionNew digital treatment formats may reduce barriers to treatment for individuals with suicidal ideation. This study aimed to investigate the feasibility of a remote blended care programme for this population, defined as acceptability, demand, practicality, adaptation, indications of efficacy and safety.MethodsWe conducted a mixed‐methods single‐arm trial for proof‐of‐concept. Participants were eligible if they were at least 18 years old, had sufficient German proficiency, a Beck Scale for Suicidal Ideation score ≥2, internet access and lived near the outpatient clinic. The treatment consisted of 12 sessions of cognitive‐behavioural videotherapy combined with online modules over 6 weeks.ResultsWe included 10 participants. All patients were satisfied with the treatment; most patients (80%) reported unpleasant memories resurfacing. All patients completed all therapy sessions and a mean of 13.7 modules (SD = 5.7); three patients switched to face‐to‐face treatment, in one case due to safety concerns. All patients and most therapists (83.3%) found the treatment overall practicable. Most patients (66.7%) and therapists (66.7%) considered remote treatment equivalent to face‐to‐face therapy. There were no serious adverse events.ConclusionWhile promising, the results suggest changes to the programme might be needed, particularly for patients' safety. A controlled feasibility trial should investigate temporary deteriorations.

Publisher

Wiley

Subject

Clinical Psychology

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