Study Stopped
With change of personnel and lab resources, this study was not feasible without independent funding
Effects of Cognitive and Emotional Functioning on Treatment Outcomes
CEO
An Investigation of the Effects of Cognitive and Emotional Functioning on Treatment Outcomes
1 other identifier
interventional
N/A
1 country
1
Brief Summary
The investigators are interested about the degree to which individuals can persist with individualized treatment goals when their cues (external such as food, or internal such as anxiety) are high for impulsive/maladaptive behavior (e.g., purging, not eating, etc.). The investigators want to find specific high-difficulty situations in which to assess whether participants remain mindful of the big picture and are willing to work toward therapeutic goals. Also, the investigators want to rate the participants degree of success (e.g., proportion of calories eaten) assessed more objectively. The theory is that working memory capacity (WMC) modulates the ability to keep longer-term goals in mind when faced by current stress/temptations. For example, the ability to control drinking when one has an implicit urge to drink is predicted by WMC. The ability to apply a novel emotional regulation skill at a time of stress is also predicted by WMC. Indeed, the generic ability to pursue goals in the future (as assessed by the discounting of the value of future goals) is reliably predicted by WMC. There is also evidence that activation of brain regions associated with WMC (by direct activation of the dorsolateral prefrontal cortex via transcranial magnetic stimulation (TMS), or by having a person complete a relevant cognitive task) improves delay discounting. Accordingly, the investigators are proposing a study that both assesses the link between WMC and relevant the clinical measures noted above, as well as changes in these measures following activation of WM with a cognitive prime (WM task). The overall design calls for an initial WMC assessment, followed by randomization to complete 3 days of a WM prime and then 3 days of a no prime group, or vice versa. The investigators then assess the clinical outcomes noted above across the following 6 days, with a WM prime first or no prime first occurring prior to the targeted behaviors. The investigators will prime WM prior to participant's evening meal, with the WM intervention offered during the free time before this meal.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Sep 2019
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 2, 2017
CompletedFirst Posted
Study publicly available on registry
February 13, 2017
CompletedStudy Start
First participant enrolled
September 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2022
CompletedJuly 10, 2019
July 1, 2019
3.2 years
January 2, 2017
July 8, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Meal Compliance
Therapeutic Food and Snack Log.
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Secondary Outcomes (5)
Mood
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Delay Discounting
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Eating Disorder Symptoms
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Depression
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Depression, Anxiety, and Stress
Comparison of day 5 to day 8 scores taking into account intervention type, intervention order, and baseline scores
Study Arms (2)
Working Memory Intervention (N-back)
EXPERIMENTALParticipants will complete the working memory priming task either for the first 3 days of the intervention or the last 3 days of the intervention, with order counterbalanced across participants. The working memory prime is the N-back test, a measure of working memory in which individuals need to make a response to targets which are repeated letters either in a row (i.e., one-back) or in every-other-letter format (i.e., two-back) (Jaeggi et al., 2010).
"White Bear" Task
PLACEBO COMPARATORParticipants will complete this non-working-memory control task either for the first 3 days of the intervention or the last 3 days of the intervention, depending on counterbalanced order. The task consists of a procedure developed by Wegner and colleagues (1987) in a study of thought suppression, which instructs participants to inhibit thoughts of a white bear, and to indicate with a pencil mark every time the thought of the white bear occurs to them.
Interventions
The N-back task is a measure of working memory in which individuals need to make a response to targets which are repeated letters either in a row (i.e., one-back) or in every-other-letter format (i.e., two-back).
For this thought suppression task, participants are instructed to inhibit thoughts of a white bear, and to indicate with a pencil mark every time the thought of the white bear occurs to them.
Eligibility Criteria
You may qualify if:
- Residential patients
- Females 18 and older
- Able to provide informed consent for the study
- Sufficient command of the English language
- Have experience using a computer and mouse
- Diagnosed with an Eating Disorder
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Boston University
Boston, Massachusetts, 02215, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Psychology
Study Record Dates
First Submitted
January 2, 2017
First Posted
February 13, 2017
Study Start
September 1, 2019
Primary Completion
November 1, 2022
Study Completion
December 1, 2022
Last Updated
July 10, 2019
Record last verified: 2019-07
Data Sharing
- IPD Sharing
- Will not share