Managing Our Relationship With Food & Eating

Status Completed

Clinical Trial Summary

There is a need for population-level intervention research to address the impacts of the COVID-19 pandemic on disordered eating and unhealthy eating behaviours. Systematic reviews have demonstrated that psychotherapy and yoga can help to reduce binge eating and disordered eating habits, however, these interventions were tested in person. Studies examining the effectiveness of these interventions in an online, group-based format are warranted. In 2019, the investigators launched a RCT to test gender-stratified group interventions to address mental health and addictive behaviours among community-based adults in southern Alberta. The investigators implemented this intervention with more than 200 adults in person before this study was paused due to COVID-19; In 2020, the investigators adapted this intervention for online delivery to 200 community-dwelling women across Alberta. The most recent iteration of this study indicated the participants were particularly concerned about their relationship with food and how they were engaging in different eating behaviours to cope with the stress of COVID-19.

Clinical Trial Description

The primary objective of this project is to adapt two existing mental health and substance use interventions and RCT for online delivery to address unhealthy eating behaviours and a negative relationship with food for women within the context of COVID-19. The second objective is to test if an online group body-oriented intervention (trauma-sensitive yoga) that has been designed to increase awareness of physical sensations, is superior to an online group verbal narrative intervention (mental wellness talking circle), and to control group. The investigators theorize that the body-oriented intervention may offer the opportunity to reprogram automatic physiologic hyperarousal in response to COVID-19 triggers and increase positive body awareness, and mindful attention to the ways in which habitual self-protective behaviours, like unhealthy eating behaviours, may be impacting health. The third objective is to examine the impacts of the interventions on adults with pre-existing mental health and disordered eating issues, and those with previous experiences that may make them more susceptible to these problems during COVID-19. The investigators will track other supports they engage in during the study and the perceived impacts of these supports on their outcomes with the goal of shedding light on how to best match COVID-19 related services to adults who need them the most. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04797689
Study type	Interventional
Source	University of Lethbridge
Contact
Status	Completed
Phase	N/A
Start date	April 1, 2021
Completion date	July 22, 2021

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT04549194` - Contribution of L-Tyrosine to Recovery From Operational Strain on Return From External Operation	N/A
Completed	`NCT04053686` - An Intervention to Reduce Prolonged Sitting in Police Staff	N/A
Completed	`NCT03170752` - Implementing and Testing a Cardiovascular Assessment Screening Program (CASP)	N/A
Recruiting	`NCT05419934` - EMDR Therapy in Young Children, a Double-blinded Randomized Controlled Trial	N/A
Completed	`NCT03689348` - Acute and Chronic Effects of Avena Sativa on Cognition and Stress	N/A
Active, not recruiting	`NCT05114824` - Acceptability and Feasibility of an 8-week Online Mindfulness-Based Cognitive Therapy Program Among Undergraduate Students	N/A
Recruiting	`NCT05991739` - Pilot Testing of a Structural Racism Intervention for Immigrant Latinx Families	N/A
Not yet recruiting	`NCT05491122` - The Influence of Fluid Intake on Daily Biological Rhythm and Mental Performance in Healthy Young Adults	N/A
Completed	`NCT02982070` - TU Tough: Mental Toughness Training for College Success	N/A
Completed	`NCT02844478` - Stress-Busting Program and QoL, Bio-markers of Immunity/Stress and Cellular Aging	N/A
Completed	`NCT02417454` - Study on the Effects of a Probiotic on Autonomic and Psychological Stress	Phase 3
Completed	`NCT06014970` - The Health and Wellness Curriculum Assessment	N/A
Completed	`NCT01946893` - Mindfulness Meditation for Cognition and Mood	N/A
Completed	`NCT01637363` - Psychoeducation to Sick-listed Individuals With Mental Health Problems	N/A
Completed	`NCT01343810` - Stress Reduction Training to Improve Sleep Quality, Stress Physiology & Cardiovascular Disease (CVD) Risk Markers	N/A
Completed	`NCT00661271` - Mindfulness-based Stress Reduction for Urban Youth	N/A
Recruiting	`NCT04417153` - Who Benefits More? Optimising Mindfulness Based Interventions for Improved Psychological Outcomes
Completed	`NCT04125810` - A Study to Assess the Safety and Efficacy of Probiotic to Modulate Psychological Stress	Phase 2
Completed	`NCT04023968` - Student Wellness Workshop Study	N/A
Completed	`NCT03233750` - Simulation-Based Stress Inoculation Training	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Managing Our Relationship With Food and Eating — NOURISH

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms