Brain training for eating disorders: a new hope?
NCT ID NCT03808467
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a type of therapy called cognitive remediation therapy (CRT) for women with eating disorders like anorexia, bulimia, or binge-eating disorder. CRT aims to improve thinking skills such as flexibility, planning, and impulse control, which are often affected in these conditions. One hundred women who are already in treatment and have certain thinking difficulties will receive nine weekly CRT sessions. Researchers will measure changes in thinking, eating disorder symptoms, and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cognitive remediation therapy (CRT)
- What this could lead to
- If it works, this could provide an additional therapy to help people with eating disorders think more flexibly and improve their symptoms.
- What could go wrong
- This is a relatively small, early-stage trial. The therapy may not show significant benefits, and results may not apply to all eating disorder patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2019
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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16 to 36 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Being in in-patient-, day- or out-patient treatment for an eating disorder (anorexia nervosa, bulimia nervosa, binge eating disorder or OSFED) * Displaying cognitive difficulties (score ≤ -1 standard deviation) on: 1. the Inhibit, Shift, Plan/ Organize and/ or Global Executive Composite indexes of the self-report measure the BRIEF-A (reversed) 2. the Total errors, Perseverative Responses, Perseverative Errors and/ or Learning to learn from the Wisconsin Card Sorting Test (WCST) and/ or on the Rey Complex Figure Test (RCFT) Copy condition or Q-score and/ or on condition 3 and 4 on the Color-word Interference Test from (D-KEFS) * Being able to understand and speak Norwegian * Be willing to provide written informed consent * Accepting random allocation to the two arms of the study Exclusion Criteria: * A history of congenital or acquired brain injury (except concussions) * Active substance abuse * Psychosis * Intelligence quotient (IQ) less than 70
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of Psychology, Norwegian University of Science and Technology
Trondheim, N-7491, Norway
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Levanger Hospital, Nord-Trøndelag Hospital Trust
Levanger, N-T, Norway
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St Olavs Hospital HF
Trondheim, Norway
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