Actively Recruiting
Impact of an Intervention with a Narrative Approach in Overusers: a Clinical Trial
Led by Catalan Institute of Health · Updated on 2024-08-26
264
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare an intervention with a narrative therapy-based approach with standard care in overusers in general practice . The main question it aims to answer are: • An intervention with an approach based on narrative therapy can improve the perception of emotional support, and reduce the probability of suffering from anxiety and/or depression, the number of consultations, and the number of medications in primary care overusers. Participants will 10 individual sessions carried out over five months. The interval between sessions will be two weeks with a specific duration of fifty minutes per session.. If there is a comparison group: Researchers will compare two groups of overusers to see if reduces the number of visits to the primary care doctor.
CONDITIONS
Official Title
Impact of an Intervention with a Narrative Approach in Overusers: a Clinical Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Users in the 95th percentile in the distribution of face-to-face, patient self-initiated consultations with primary healthcare services within 1 year
- Aged between 25 and 85 years
You will not qualify if you...
- Drug abuse or dependence, except for nicotine and tetrahydrocannabinol
- Severe mental disorders as defined by DSM-IV-TR
- Severe cognitive disorders or sensory disabilities as defined by ICD-10
- Major locomotor mobility limitations or terminal illness
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Centre d'Atenció Primària Montnegre, Institut Català de la Salut, Barcelona, Catalonia, Spain
Barcelona, Catalonia, Spain, 08029
Actively Recruiting
Research Team
V
Valentin Calvo-Rojas Phd, Social Worker
CONTACT
C
Calvo-Rojas Phd, Social Worker
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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