1. App-Delivered Cognitive-Behavioral Therapy for Insomnia Among Patients with Comorbid Musculoskeletal Complaints and Insomnia Referred to 4-Week Inpatient Multimodal Rehabilitation: Protocol for a Randomized Clinical Trial
- Author
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Skarpsno,Eivind Schjelderup, Simpson,Melanie Rae, Seim,Arnfinn, Hrozanova,Maria, Bakøy,Marthe, Klevanger,Nina, Aasdahl,Lene, Skarpsno,Eivind Schjelderup, Simpson,Melanie Rae, Seim,Arnfinn, Hrozanova,Maria, Bakøy,Marthe, Klevanger,Nina, and Aasdahl,Lene
- Abstract
Eivind Schjelderup Skarpsno,1,2 Melanie Rae Simpson,1 Arnfinn Seim,1,3 Maria Hrozanova,1 Marthe Alida Bakøy,3 Nina Elisabeth Klevanger,1 Lene Aasdahl1,3 1Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway; 2Department of Neurology and Clinical Neurophysiology, St. Olavs Hospital, Trondheim, Norway; 3Unicare Helsefort Rehabilitation Centre, Rissa, NorwayCorrespondence: Eivind Schjelderup Skarpsno, Department of Public Health and Nursing, NTNU, Trondheim, Norway, Tel +47 97521297, Email eivind.s.skarpsno@ntnu.noBackground: Insomnia is prevalent among patients receiving treatment for long-term musculoskeletal complaints in inpatient rehabilitation settings. Cognitive-behavioral therapy for insomnia (CBT-I) is effective for improving sleep quality in patients with pain, but a lack of therapists often limits the capacity to use this therapy in rehabilitation programs. The aim of this randomized clinical trial (RCT) is to evaluate the effectiveness of app-delivered CBT-I adjunct to inpatient multimodal rehabilitation for individuals with comorbid musculoskeletal complaints and insomnia, compared with rehabilitation (usual care) only.Methods: This RCT has two parallel arms: 1) inpatient multimodal rehabilitation and 2) app-delivered CBT-I adjunct to inpatient multimodal rehabilitation. Patients referred to Unicare Helsefort (Norway) with long-term chronic musculoskeletal complaints are invited to the study. Eligible and consenting participants will be randomized to the intervention and usual care at a ratio of 2:1. Assessments will be carried out at baseline (prior to randomization), 6 weeks (at the end of rehabilitation), 3 months (primary outcome), as well as 6 and 12 months after the rehabilitation. The primary outcome is insomnia severity measured at 3 months. Secondary outcomes include pain intensity, health-related quality of life, fatigue, physical function, work abilit
- Published
- 2023