Psychosocial factors linked to outcomes in people with dual diagnosis in a hospital

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a cross-sectional observational study conducted at a single general hospital. It will enroll adults hospitalized with a dual diagnosis and collect sociodemographic, clinical, and psychosocial data from routine assessments and medical records. Standardized instruments will be used to measure psychosocial protective factors and clinical-functional outcomes to explore their associations. No experimental intervention is involved; the goal is to better understand factors that may influence severity and recovery in this population. Findings may inform treatment planning and care strategies in hospital settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults (≥18 years).
* Hospitalized patients with a clinical diagnosis of dual diagnosis.
* Ability to provide informed consent.

Exclusion Criteria:

* Severe cognitive impairment or acute clinical condition preventing assessment.
* Refusal or inability to provide informed consent.

Where it's running

• Hospital Virgen del Puerto
  Plasencia, Caceres, Spain Recruiting

Study contacts

• Study coordinator: Guillermo F Martínez Montás, MD
• Email: guillermof.martinez@salud-juntaex.es
• Phone: +34689617510

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Virtual Reality to Help Youth in Residential Care Reduce Alcohol and Cannabis Use

  This trial tests whether a virtual reality intervention can boost self-confidence to resist drinking and cannabis use among youths in residential care with co-occurring disorders.

  Recruiting Universidad Francisco de Vitoria · Pozuelo de Alarcón, Madrid · NCT07834606

• Trauma-focused group therapy for adults with trauma symptoms in primary care

  A group-based trauma therapy delivered in primary care to see if it helps adults with trauma-related symptoms more than usual care.

  Recruiting University Ramon Llull · Barcelona, Barcelona · NCT07757334

• Honest, Open, Proud for justice-involved veterans

  This trial tests a peer-delivered stigma-reduction program for veterans with co-occurring mental health or substance use disorders who are involved with the justice system, to see if different delivery intensities help more veterans engage in care.

  Recruiting VA Office of Research and Development · Bedford, Massachusetts · NCT07742722

• Does extra family income improve child mental health and brain biology in low-income families?

  This study tests whether three years of extra income for parents can improve their child’s mental health and neuroimmune function.

  Recruiting Northwestern University · Evanston, Illinois · NCT07641244

• Olfactory function and decision-making in people with HIV and/or substance use

  This study tests how the sense of smell relates to decision-making in adults with HIV, substance use, both, or neither.

  Recruiting National Institutes of Health Clinical Center (CC) · Baltimore, Maryland · NCT07637669

• Understanding and Targeting Self-Regulatory Control in Bulimia Nervosa

  In women with bulimia nervosa, this study tests whether real-time brain feedback during eating, paired with a 4-week text-message program, can help improve self-control and reduce symptoms.

  Recruiting Icahn School of Medicine at Mount Sinai · New York, New York · NCT07581158

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.