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Testing an early online intervention for the treatment of disturbed sleep during the COVID-19 pandemic in self-reported good and poor sleepers (Sleep COVID-19): study protocol for a randomised controlled trial.
Sawdon, Olivia L; Elder, Greg J; Santhi, Nayantara; Alfonso-Miller, Pamela; Ellis, Jason G.
  • Sawdon OL; Northumbria Sleep Research, Northumbria University, Newcastle upon Tyne, NE1 8ST, UK.
  • Elder GJ; Northumbria Sleep Research, Northumbria University, Newcastle upon Tyne, NE1 8ST, UK. g.elder@northumbria.ac.uk.
  • Santhi N; Northumbria Sleep Research, Northumbria University, Newcastle upon Tyne, NE1 8ST, UK.
  • Alfonso-Miller P; Northumbria Sleep Research, Northumbria University, Newcastle upon Tyne, NE1 8ST, UK.
  • Ellis JG; Northumbria Sleep Research, Northumbria University, Newcastle upon Tyne, NE1 8ST, UK.
Trials ; 22(1): 913, 2021 Dec 11.
Article in English | MEDLINE | ID: covidwho-1571922
ABSTRACT

BACKGROUND:

Theoretical models of insomnia suggest that stressful life events, such as the COVID-19 pandemic, can cause acute insomnia (short-term disruptions to sleep). Early interventions may prevent short-term sleep problems from progressing to insomnia disorder. Although cognitive behavioural therapy for insomnia (CBT-I) is effective in treating insomnia disorder, this can be time and resource-intensive. Further, online interventions can be used to deliver treatment to a large number of individuals. The objective of this study is to investigate if an online behavioural intervention, in the form of a leaflet, which has been successfully used alongside CBT-I for acute insomnia, can reduce symptoms of acute insomnia in poor sleepers.

METHODS:

A total of 124 self-reported good and poor sleepers will be enrolled in an online stratified randomised controlled trial. After baseline assessments (T1), participants will complete a 1-week pre-intervention sleep monitoring period (T2) where they will complete daily sleep-diaries. Poor sleepers (n = 62) will be randomly allocated to an invention or wait-list group, where they will receive the intervention (T3), or will do so after a 28-day delay. Good sleepers (n = 62) will be randomly assigned to an intervention or no intervention group. All participants will complete a 1-week post intervention sleep monitoring period using daily sleep diaries (T4). Participants will be followed up at 1 week (T5), 1 month (T6) and 3 months (T7) post intervention. The primary outcome measure will be insomnia severity, measured using the Insomnia Severity Index. Secondary outcome measures will include subjective mood and subjective sleep continuity, measured using sleep diaries. Data will be analysed using an intention-to-treat approach.

DISCUSSION:

It is expected that this online intervention will reduce symptoms of acute insomnia in self-reported short-term poor sleepers, and will also prevent the transition to poor sleep in good sleepers. We expect that this will demonstrate the feasibility of online interventions for the treatment and prevention of acute insomnia. Specific advantages of online approaches include the low cost, ease of administration and increased availability of treatment, relative to face-to-face therapy. TRIAL REGISTRATION ISRCTN43900695 (Prospectively registered 8th of April 2020).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Internet-Based Intervention / COVID-19 Type of study: Experimental Studies / Prognostic study / Qualitative research / Randomized controlled trials Limits: Humans Language: English Journal: Trials Journal subject: Medicine / Therapeutics Year: 2021 Document Type: Article Affiliation country: S13063-021-05888-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Internet-Based Intervention / COVID-19 Type of study: Experimental Studies / Prognostic study / Qualitative research / Randomized controlled trials Limits: Humans Language: English Journal: Trials Journal subject: Medicine / Therapeutics Year: 2021 Document Type: Article Affiliation country: S13063-021-05888-0