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INTERACT-AN: enhancing arousal regulation in people with post-traumatic stress disorder tijdens Anorexia Nervosa

INTERACT-AN: The implementation of a body-focused INTERvention, enhancing Arousal regulation in patients with Comorbid post-Traumatic stress disorder during Anorexia Nervosa: an intervention study. - INTERACT-AN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON61291
Enrollment
24
Registered
2026-01-16
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Eating disorder

Interventions

Participants will engage in the body-oriented intervention “Arousal Regulation”, which consists of eight weekly individual sessions of 60 minutes led by a (psychomotor) therapist experienced in workin

Sponsors

GGNet
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients are eligible for inclusion in the study if they meet all of the following criteria:Participation in inpatient eating disorder treatment.A current diagnosis of AN according to DSM-5 criteria. AN will be diagnosed by a licensed psychologist during an intake assessment by using the SCID-5-S interview.A comorbid diagnosis of PTSD according to DSM-5 criteria. PTSD will be assessed by a licensed psychologist during the intake assessment by using the SCID-5-S interview. Age 18 years and above.Demonstrated willingness to participate, confirmed by signing written informed consent.

Exclusion criteria

Exclusion criteria: Patients will be excluded from the study if they meet any of the following criteria:Current psychotic or manic episode.Severe substance use disorder (moderate or severe, based on DSM-5 criteria) that could interfere with treatment participation.Acute suicidality or self-harming behaviour requiring immediate crisis intervention or a higher level of care.Significant cognitive impairment or intellectual disability that would impede comprehension of the intervention or participation in assessments.Insufficient proficiency in Dutch, preventing adequate participation in treatment and study procedures.Medical instability or acute physical health problems that contraindicate participation in psychological treatment.Participation in another clinical trial that could interfere with the outcomes or procedures of the current study.

Design outcomes

Primary

MeasureTime frame
The primary study outcome, feasibility, will be assessed on the five domains of 1) acceptability (Client Satisfaction Questionnaire (CSQ-8)); 2) demand (rate of participant enrolment); 3) implementation (drop-out, adherence and treatment integrity); 4) adaptation (Tops and Tips); and 5) preliminary efficacy (Multidimensional Assessment of Interoceptive Awareness – Version 2 (MAIA-2), Difficulties in Emotion Regulation Scale (DERS), Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5)).

Countries

Netherlands

Contacts

Public ContactSHW Mares

GGNet

s.mares@ggnet.nl0625743442

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 3, 2026