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Effectiveness of a Stress Reduction Intervention for Disordered Eating Behaviours

Evaluation of a smartphone-based stress reduction intervention for reducing episodes of disordered eating among women who engage in stress-related eating behaviours.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000432112
Enrollment
227
Registered
2019-03-18
Start date
2019-07-06
Completion date
2019-09-23
Last updated
2020-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The proposed study aims to evaluate the efficacy of a stress-reduction intervention for unhealthy and disordered eating behaviours. The study will be conducted as a randomised control trial, with a wait-list control group and two intervention groups; one intervention group will be prompted to use the intervention, whilst the other will not. All groups will complete a baseline survey, followed by four weeks of ecological momentary assessment to obtain data regarding their eating behaviours and affect. During this time, the intervention groups will also be provided with brief stress-reduction activities via smartphone application that they can complete when stressed. Participants in the intervention groups will also complete a four-week follow-up survey. The study will recruit at least 183 women, aged 18 years and over, who report stress-related unhealthy or disordered eating. It is expected that use of the intervention will reduce the momentary and longer-term risk of disordered eating.

Interventions

Brief name: Stress reduction intervention. The intervention will involve a series of brief 3-5 minute stress reduction activities that are delivered via a smartphone application ('app'). These activities are audio files which included guided meditations, breathing exercises, thought defusion (letting go of thoughts), body scans, and gratitude exercises. There will be two intervention groups: guided and self-guided. Once access to the app is provided, participants in both groups will be able

Brief name: Stress reduction intervention. The intervention will involve a series of brief 3-5 minute stress reduction activities that are delivered via a smartphone application ('app'). These activities are audio files which included guided meditations, breathing exercises, thought defusion (letting go of thoughts), body scans, and gratitude exercises. There will be two intervention groups: guided and self-guided. Once access to the app is provided, participants in both groups will be able to access the stress-reduction activities whenever they choose. However, it is recommended that participants use these activities at times when they are feeling stressed. Participants in the guided intervention group will also receive personalised prompts to remind them to use the app; these are delivered when participants report they are at least moderately stressed. This reporting occurs via periodic surveys prompted through the same app; these are delivered 4 times per day at randomised times between the hours of 9am to 9pm for the four week duration of the study. The survey comprises only one question ("How stressed are you right now?"). Participants in the self-guided intervention group will also complete this monitoring and have access to the stress-reduction activities to use whenever they choose, however they will not receive any personalised reminders. The intervention phase of the study will last for four weeks. Participants' use of the intervention will be monitored through the app, in which participants will be asked to respond to a brief one-item survey prior to and after using a stress-reduction activity. As the activities are delivered via the app, it is not possible to directly assess fidelity. Adherence will be promoted through provision of a variety of different exercises to allow participants to engage with those they find most helpful and reduce the likelihood of disinterest due to repetition.

Sponsors

A/Prof Matthew Fuller-Tyszkiewicz
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Identify as a woman, aged 18 years and over, own a smartphone, engage in stress-related eating behaviours, this may include eating mindlessly, non-hungry eating, eating foods one may normally choose to avoid, overeating, feeling a sense of loss of control over one’s eating, and binge eating.

Exclusion criteria

None

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026