The Say No study - a study to reduce indulgent foods in adults.

Not Applicable

Completed

• Conditions: overweight; Public Health - Health promotion/education; Diet and Nutrition - Obesity

• Registration Number: ACTRN12616001239459
• Lead Sponsor: niversity of Sydney

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-09-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

Participants must be aged greater than or equal ro 18 years with a BMI greater than or equal to 25 kg/m2
Participants would like to reduce the number of indulgent foods and drinks they have.

Exclusion Criteria

Pregnant or intending to fall pregnant within the study time period.
Current eating disorder or medical history of eating disorders.
Taking part in a clinical weight loss trial.
Currently attending a weight management programme (including pharmacotherapy or current/previous bariatric surgery).
Use of weight loss medications and other drugs that may affect body weight e.g. anti-psychotics, anti-depressants, or corticosteroids.
A history or presence of malignancy [completely resected basal or squamous cell carcinoma of the skin if treatment completed > 6 months prior to enrolment and Participant is in remission for > 5 years prior to Screening remain eligible].

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The participants will be asked to record the number of self-defined indulgences for seven days prior to attending the baseline appointment and for seven days starting at week seven (end of intervention). Participants will be asked to record the time of the indulgence and a description of the indulgence. The primary outcome is the change in the number of indulgences between the intervention groups and control group. [Change between baseline and 8 weeks]