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TRANPAS - TReating Anorexia Nervosa Plus Autism Spectrum

Not Applicable
Not yet recruiting
Conditions
Anorexia Nervosa
Autism Spectrum Disorder
Interventions
Other: Anorexia nervosa plus autism
Registration Number
NCT06368687
Lead Sponsor
Göteborg University
Brief Summary

In a pilot study, the investigators will validate a so-called autism care location in an inpatient ward. The care location will be adapted for patients with anorexia nervosa (AN) and concurrent autism (AN+autism). In order to investigate the effect of a tailored care location for patients with AN + autism, the evaluation will include weight development and changes in nutritional intake, eating disorder and anxiety symptoms. The overall aim is to improve treatment for this specific AN subgroup, that otherwise has a worse prognosis regarding AN recovery.

Detailed Description

Anorexia nervosa (AN) is a serious eating disorder and has the highest mortality rate of all psychiatric illnesses. Adolescence is the most common age of onset. Nine out of ten people who fall ill are girls/women, and 2% of all girls/women will fall ill with AN at some point in their lives. In AN, one engages in self-starvation, which in turn leads to underweight. 75 - 80% of individuals with AN recover during adolescence, while the remainder are at high risk of developing chronic AN. For the individual, the chronic condition means great suffering in the form of serious psychiatric and somatic co-morbidity, social isolation and reduced/lack of work ability. People with autism show social withdrawal and reduced flexibility, reminiscent of the symptoms seen in AN. An estimated 15 - 20% of all individuals with AN also have autism. People with AN and concurrent autism run an increased risk of a worse prognosis, as they have more difficulty absorbing treatment, which in itself increases the risk of the condition becoming chronic. Today, there is no scientific evidence for how people with AN and concurrent autism should be treated.

In a pilot study, the investigators will validate a so-called autism care location in our inpatient ward, at Sahlgrenska University Hospital in Gothenburg, Sweden. The care location will be adapted for patients with AN and concurrent autism (AN+autism). In order to investigate the effect of a tailored care location for patients with AN + autism, the evaluation will include weight development and changes in nutritional intake, eating disorder and anxiety symptoms. The overall aim is to improve treatment for this specific AN subgroup, that otherwise has a worse prognosis regarding AN recovery.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
10
Inclusion Criteria
  • 25 years or older
  • Meeting criteria for both anorexia nervosa and autism spectrum disorder according to the DSM-5
  • In need of inpatient care due to anorexia nervosa
Exclusion Criteria
  • 24 years or younger
  • Not in need of inpatient care due to anorexia nervosa
  • Not meeting criteria for both anorexia nervosa and autism spectrum disorder according to the DSM-5

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Anorexia nervosa plus autismAnorexia nervosa plus autismThe treatment model takes into account the patient's perception disorders. This means e.g. an adapted mealtime situation where the patient can eat separately or wear hearing protection if necessary. The patients have an adapted meal plan regarding difficulties with specific textures or foods. To meet their need for continuity, they have the same contact persons throughout the entire period of care. The healthcare staff receive training in working with the specific subgroup and have regular exchanges of experience regarding the patient group, 15 minutes every or every two weeks.
Primary Outcome Measures
NameTimeMethod
BMI change between baseline and discharge 12 weeks laterAt admission, at discharge 12 weeks later, and 6 months after discharge

Body Mass Index: weight (kilograms)/height (meters)2

Secondary Outcome Measures
NameTimeMethod
Change of level of anxiety between baseline and discharge 12 weeks laterAt admission, at discharge 12 weeks later, and 6 months after discharge

Anxiety assessed using General Anxiety Disorder 7-item (GAD-7)

Change of Quality of life between baseline and discharge 12 weeks laterAt admission, at discharge 12 weeks later, and 6 months after discharge

Quality of life (QoL) assessed using Short Form Health Survey (SF-36)

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