A randomized controlled trial to compare the effects of time-restricted eating vs. Mediterranean diet on symptoms and quality of life in bipolar disorder

Author:

Johnson Sheri L1,Murray Greg2,Kriegsfeld Lance J.1,Manoogian Emily3,Mason Liam4,Allen J. D.1,Berk Michael5,Panda Satchidanda3,Rajgopal Nandini A.6,Gibson Jake C.1,Joyner Keanan1,Villanueva Robert1,Michalak Erin E.6

Affiliation:

1. University of California, Berkeley

2. Swinburne University of Technology

3. Salk Institute for Biological Studies

4. City, University of London

5. Deakin University

6. University of British Columbia

Abstract

Abstract Background: The primary objective of this randomized controlled trial (RCT) is to establish the effectiveness of time-restricted eating (TRE) compared with the Mediterranean diet for people with bipolar disorder (BD) who have symptoms of sleep disorders or circadian rhythm sleep-wake disruption. This work builds on the growing evidence that TRE has benefits for improving circadian rhythms. TRE and Mediterranean diet guidance will be offered remotely using self-help materials and an app, with coaching support. Methods: This study is an international RCT to compare the effectiveness of TRE and the Mediterranean diet. Three hundred participants will be recruited primarily via social media. Main inclusion criteria are: receiving treatment for a diagnosis of BD I or II (confirmed via MINI structured diagnostic interview), endorsement of sleep or circadian problems, self-reported eating window of ≥ 12 hours, and no current mood episode, acute suicidality, eating disorder, psychosis, alcohol or substance use disorder, or other health conditions that would interfere with or limit the safety of following the dietary guidance. Participants will be asked to complete baseline daily food logging for two weeks and then will be randomly allocated to follow TRE or the Mediterranean diet for 8 weeks, during which time, they will continue to complete daily food logging. Intervention content will be delivered via an app. Symptom severity interviews will be conducted at baseline; mid-intervention (4 weeks after the intervention begins); end of intervention; and at 3, 6, and 12 months postintervention by phone or videoconference. Self-rated symptom severity and quality of life data will be gathered at those timepoints, as well as at 6 weeks postintervention. To provide a more refined index of whether TRE successfully decreases emotional lability and improves sleep, participants will be asked to complete a sleep diary (core CSD) each morning and complete six mood assessments per day for eight days at baseline and again at mid-intervention. Discussion: The planned research will provide novel and important information on whether TRE is more beneficial than the Mediterranean diet for reducing mood symptoms and improving quality of life in individuals with BD who also experience sleep or circadian problems. Trial registration: ClinicalTrials.gov: ID: 2022-10-15725. Pending, submitted 12/17/2023.

Publisher

Research Square Platform LLC

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