University of California San Francisco
San Francisco, California, 94143, United States
NCT Number: NCT02694731
Participants will complete a 5-week smartphone app-based intervention that teaches mindful eating skills. One goal is to determine to what extent participants will enjoy using the app and complete the intervention. The investigators predict that after completing the intervention, participants will report fewer episodes of eating in response to food cravings. The investigators will also measure several other biological and behavioral outcomes.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
San Francisco, California, 94143, United States
In this prospective repeated-measures cohort study, participants will complete a 5-week smartphone app-based intervention that teaches mindful eating skills. The investigators will assess psychological and behavioral intervention targets using questionnaires and brief mobile assessments. The investigators will also measure BMI and adiposity. Assessments will occur at pre-intervention, post-intervention, and 1 and 2 months post intervention. At several times during the study, participants will also receive multiple daily text messages asking them to complete a brief food craving assessment on their phone. This "experience sampling" approach is critical as it allow the investigators to capture experiences and behaviors that are often brief and automatic, making them poorly suited to traditional retrospective questionnaires. The investigators will also assess acceptability and continued use of the app via anonymous usage logs.
Overall, the aims are to 1) assess feasibility of the protocol, 2) assess changes in food cravings and indulgence of cravings, and 3) determine the extent to which participants remain engaged with the app after completing the 5-week intervention period and whether this predicts maintenance of benefits at 1 month and 2 months post-intervention. An exploratory aim is to measure the effects of the intervention on body weight, bodyfat, and bodyfat distribution.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Consists of the app described in the arm description.
Time frame: 1 month post-intervention
Cell phone questionnaires assess frequency with which participants eat in response to food cravings. Cell phone questionnaires assess frequency with which participants eat in response to food cravings. Participants are asked whether they ate in response to a craving in the past hour
Time frame: Administered 9 times over the 7 days after the participant completes the intervention (typically 28 days after beginning the study; may be longer if participant takes extra days to complete the intervention)
Cell phone questionnaires assess frequency with which participants eat in response to food cravings. Participants are asked whether they ate in response to a craving in the past hour
Time frame: 1 month post-intervention
Questionnaire measure of drive to eat for hedonic properties of food
Time frame: immediate post-intervention (within 7 days of completing the intervention)
Questionnaire measure of drive to eat for hedonic properties of food
Time frame: 1 month post-intervention
Questionnaire measure of drive to eat for coping
Time frame: Immediate post-intervention (within 7 days of completing the intervention)
Questionnaire measure of drive to eat for coping
Time frame: 1 month post-intervention
Questionnaire measure of food cravings
Time frame: Immediate post-intervention (within 7 days of completing the intervention)
Questionnaire measure of food cravings
University of California, San Francisco
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07079046
Appetite Regulation, Behavior
Valencia, Spain
View Trial DetailsNCT06945731
Body Weight, Food Cravings
Larissa, Thessaly, Greece
View Trial DetailsNCT07056036
Behavior, Food Cravings
Denver, Colorado, United States
View Trial DetailsNCT06889298
Body Weight, Body Weight Changes
Klecany, Czechia
View Trial Details