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

被引:0
|
作者
Buescher, Rebekka [1 ]
Teismann, Tobias [2 ]
Hartleitner, Paula [1 ]
Klein, Jan Philipp [3 ]
Baumeister, Harald [4 ]
Sander, Lasse B. [1 ]
机构
[1] Univ Freiburg, Fac Med, Dept Med Psychol & Med Sociol, Freiburg, Germany
[2] Ruhr Univ Bochum, Mental Hlth Res & Treatment Ctr, Dept Psychol, Bochum, Germany
[3] Luebeck Univ, Dept Psychiat Psychosomat & Psychotherapy, Lubeck, Germany
[4] Ulm Univ, Inst Psychol & Educ, Dept Clin Psychol & Psychotherapy, Ulm, Germany
关键词
proof-of-concept; remote blended treatment; suicidal ideation; COGNITIVE-BEHAVIORAL THERAPY; PSYCHOMETRIC PROPERTIES; RISK-FACTORS; PSYCHOTHERAPY; INTERVENTIONS; METAANALYSIS; SATISFACTION; SCALE;
D O I
10.1002/cpp.2905
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
IntroductionNew 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 & GE;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.
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页数:13
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