A Mixed-method Pilot Investigation of Paradoxical Intention for Insomnia.

Status Not yet recruiting

Clinical Trial Summary

The investigators aim to test the preliminary efficacy as well as the acceptability and feasibility of paradoxical intention, which is a psychotherapeutic technique, for improving insomnia symptoms in adults. Previous research has tested this technique for insomnia and found overall positive results. However, during the last decades very few studies have examined paradoxical intention. Therefore the investigators wish to conduct a pilot study examining the effects in a modern context.

Clinical Trial Description

In the 1970s, Ascher and Efran developed paradoxical intention (PI), instructing sleep onset insomnia patients to stay awake instead of trying to sleep. The American Academy of Sleep Medicine confirmed PI's effectiveness. However, between 2006-2018, PI use in clinical practice declined. The study will investigate PI's acceptability, mechanisms, and predictors for effectiveness. It involves a pilot trial with 40 insomnia patients in Sweden, recruited through advertisements and screened through web questionnaires, phone interviews, and sleep diaries. Criteria are based on insomnia research standards and Diagnostic and Statistical Manual Fifth Edition (DSM-5), including insomnia with common comorbidities. Participants will undergo baseline assessments, then receive four weekly online PI modules, including educational texts, behavioral experiments, and homework. Weekly therapist meetings via phone or video will support and troubleshoot issues. Post-treatment, 10-15 participants will be randomly selected for qualitative interviews to evaluate their experiences with PI, focusing on sleep patterns, text volume, therapist support, and homework's impact on sleep quality and treatment adherence. Interviews will be audio-recorded and analyzed thematically. ;

Study Design

Related Conditions & MeSH terms

Comorbidities and Coexisting Conditions
Insomnia
Sleep Initiation and Maintenance Disorders

Clinical Trial Details

NCT number	NCT06259682
Study type	Interventional
Source	Örebro University, Sweden
Contact	Annika Norell
Phone	+4619302259
Email	Annika.Norell@oru.se
Status	Not yet recruiting
Phase	N/A
Start date	April 2024
Completion date	June 2025

View Details

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