Inpatient Care of Patients With Difficult to Treat Anorexia Nervosa - Factors Affecting Treatment Outcome.
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-64
SponsorRegion Skane
About this trial
The overall aim of the project is to investigate factors that may influence treatment outcomes in people with difficult-to-treat anorexia nervosa who are enrolled in inpatient care at the Region Skåne Eating Disorders Centre in Lund. Treatment expectations, sense of autonomy, and patient participation, will be investigated, as well as caregivers' attitudes towards, and experiences of working with, autonomy and patient participation in the inpatient setting. The research project is expected to contribute to increased knowledge about the treatment of difficult-to-treat anorexia nervosa, and what part patient participation and autonomy may play when treating severe eating disorders. The overall objectives of the research program are:
1. To contribute to increased knowledge about factors that influence the treatment of people with difficult-to-treat anorexia nervosa 2. To highlight the role of autonomy and patient participation in inpatient care of severe eating disorders 3. To use the research results for clinical improvement work at Region Skåne Eating Disorders Center
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Anorexia Nervosa diagnosis (ICD F50.0)
Admitted to inpatient care at department 5 at Region Skåne Eating Disorders Center
Disqualifiers
Confidential identity
Inability to read or write in Swedish or English
Condition or treatment that, according to the study team, makes participation in the study inappropriate
Trial population
Individuals with anorexia nervosa admitted to inpatient care at Region Skåne Eating Disorders Center, a specialized psychiatric care unit for treatment of eating disorders.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Body Mass Index (BMI)
BMI is calculated using weight and height: weight (kg) / (height (m) x height (m))
Time frame
BMI will be calulated on a weekly basis throughout the inpatient treatment period, and baseline measures until end of treatment/discharge from inpatient unit at approximately 12 weeks will be used for analysis.Secondary outcomes
1
Treatment satisfaction
Satisfaction with treatment will be measured using the Client Satisfaction Questionnaire (CSQ-8), which contains 8 items. Total scores range from 8 to 32, with higher scores indicating greater satisfaction.
Time frame
CSQ-8 is collected at the end of treatment/at discharge from inpatient care at approximately 12 weeks as well at 1 year follow-up after discharge, in order to evaluate the treatment given.Locations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: