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Acquisition and Utilization of Skills Using Innovative Smartphone Application for Regular Eating

Using Ecological Momentary Interventions to Increase Skill Acquisition and Utilization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03673540
Acronym
ACQUIRE
Enrollment
61
Registered
2018-09-17
Start date
2018-08-31
Completion date
2021-01-15
Last updated
2021-09-23

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

Conditions

Binge Eating, Bulimia, Bulimia Nervosa, Eating Disorder, Purging

Keywords

Bulimia Nervosa, Eating Disorder, Binge Eating, Bulimia, Purging

Brief summary

The study seeks to evaluate the acceptability, feasibility, target engagement, and validity of an innovative smartphone application with ecological momentary interventions to augment cognitive behavioral therapy for bulimia nervosa.

Interventions

BEHAVIORALCBT+ application

Smartphone application that comprises electronic self-monitoring of food intake, eating disorder behaviors, and mood and ecological momentary interventions

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Drexel University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Meets criteria for bulimia nervosa or sub-threshold bulimia nervosa with subjective binge episodes (objective binge episodes or subjective binge episodes AND compensatory behaviors at least 1 time per week on average for the past 3 months) * BMI \>17.5 * Have a smartphone device * Willing and able to use smartphone device to track food intake multiple times per day for 16 weeks

Exclusion criteria

* Pregnant or planning to become pregnant in the next year * Currently experiencing severe psychopathology that would limit their ability to engage in study (e.g. suicidality, substance use disorder, psychotic disorder) * Have previously received a full trial of CBT for bulimia nervosa * History of bariatric surgery

Design outcomes

Primary

MeasureTime frameDescription
Binge and purge frequency assessed by the Eating Disorder ExaminationChange from baseline assessment (before beginning treatment) to post-treatment assessment (16 weeks after baseline assessment)Frequency (number of days and number of instances) of binge eating and compensatory behaviors over the past 28 days assessed by the Eating Disorder Examination

Secondary

MeasureTime frameDescription
Eating Disorder Examination Questionnaire (EDE-Q)Assessed at weekly treatment sessions throughout treatment duration (16 weeks)The Eating Disorder Examination Questionnaire measures eating pathology. The EDE-Q yields four subscale scores: Restraint, Eating Concern, Shape Concern, and Weight Concern. The possible score range for each subscale is 0 to 6. The total score may also be reported (determined by averaging the subscale scores); the score range for the total score is also 0 to 6. For subscale scores and total score, higher scores indicate more severe pathology. The restraint sub-scale of the EDE-Q will be used to assess utilization of skills related to reducing dietary restraint.
Difficulties in Emotion Regulation Scale (DERS)Assessed at weekly treatment sessions throughout treatment duration (16 weeks)The Difficulties in Emotion Regulation Scale is a self-report measure of emotional dysregulation. The DERS yields 6 subscale scores (Awareness, Clarity, Goals, Impulse, Nonacceptance, and Strategies) and a total score. The possible score range for each subscale is 3 to 15. The total score is computed by summing all 6 subscales, so the possible score range is 18 to 90. For all subscales and the total score, higher scores indicate greater difficulty in emotion regulation. The DERS will be used to assess utilization of skills related to increasing adaptive responses to cues.
Technology Acceptance Model Scale (TAMS)Assessed at weekly treatment sessions throughout treatment duration (16 weeks)The Technology Acceptance Model Scale measures usefulness and ease of use of a technological product. The TAMS yields two subscale scores (usefulness and ease of use). The possible score range for each subscale is 6 to 49. Higher scores indicate greater usefulness and ease of use. The TAMS will be used to assess the perceived usefulness and perceived ease-of-use of the smartphone application to evaluate acceptability.
Feedback Questionnaire (FQ)Assessed at weekly treatment sessions throughout treatment duration (16 weeks)The feedback questionnaire asks qualitative questions about the application. The feedback questionnaire does not report either subscale scores or a total score. The FQ will be used to obtain qualitative acceptability ratings.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026