Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

Background: The best treatment for the excessive use of the consultation is currently being discussed. Hypothesis: An intervention with an approach based on narrative therapy, compared to standard care, leads to reducing psychosocial distress and reducing the number of consultations with the family doctor. Objective: To evaluate the effectiveness of an intervention based on co-constructing a new narrative of symptoms of non-organic origin compared to usual clinical care, with respect to affective social support, the probability of suffering from anxiety and/or depression, and the use of the medical consultation. Methodology: Pragmatic, controlled and randomized, non-masked clinical trial. Study subjects: 264 users (132 in each group, intervention and control) with excessive use of the consultation (95th percentile of the distribution of appointment-type and/or urgent visits to the medicine service). Intervention will be compared with narrative approach + standard care / standard care. Determinations: Symptoms of anxiety and depression, social support, number of consultations, age, sex, marital status, educational level, income level, employment status. Statistical analysis: In order to determine the discriminant capacity of the variables associated with the intervention, we will build a multiple regression model in which we will include those that were statistically significant in the bivariate analysis and those that are relevant according to the bibliography. Expected results: The results will provide evidence on the effectiveness of said intervention. Application and Relevance: This type of intervention would most likely reduce the pressure on medical-health professionals. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06258512
Study type Interventional
Source Catalan Institute of Health
Contact Valentin Calvo-Rojas Phd, Social Worker
Phone 800-555-5555
Email valenticalvo.bcn.ics@gencat.cat
Status Recruiting
Phase N/A
Start date October 18, 2023
Completion date December 2025

See also
  Status Clinical Trial Phase
Completed NCT00042419 - Work and Health Disparities Among Rural Women N/A