Understanding behavioral addictions in patients seeking treatment
A Prospective Clinical Study of a Cohort of Pathological Patients Seeking Treatment for a Behavioral Addiction in the University Hospital of Nantes
This study looks at what influences people with behavioral addictions who are seeking treatment to see how their backgrounds and thoughts affect their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2720 (estimated) |
| Ages | 15 Years and up |
| Sex | All |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 1 site (Nantes) |
| Trial ID | NCT01248767 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the factors influencing the development and treatment adherence of patients with behavioral addictions. It will follow a cohort of individuals seeking treatment at the University Hospital of Nantes, examining various characteristics such as addictive behaviors, sociodemographic factors, clinical profiles, and cognitive distortions. The study will gather data to better understand the complexities of behavioral addictions and how they can be effectively managed.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals over the age of 15 seeking treatment for behavioral addictions at the University Hospital of Nantes.
Not a fit: Patients with cognitive impairments or those unable to read or write in French may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies for individuals struggling with behavioral addictions.
How similar studies have performed: While there have been studies on behavioral addictions, this specific observational approach focusing on treatment adherence and various influencing factors is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria : \- All consecutive patients seeking treatment at the University Hospital of Nantes for a behavioral addiction and age over 15 will be allowed to participate to the study. Exclusion Criteria : * Cognitive impairment incompatible with the assessment * Difficulty for writing or reading the French language, incompatible with the assessement * Gardianship
Where this trial is running
Nantes
- Nantes University Hospital — Nantes, France (Recruiting)
Study contacts
- Principal investigator: Marie GRALL-BRONNEC, MD — Nantes University Hospital
- Study coordinator: Gaelle CHALLET, PhD
- Email: gaelle.bouju@chu-nantes.fr
- Phone: 02.40.84.76.20
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.