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Study identifier: NCT06897410 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Reforça't: A Community, Social, and Healthcare Program for Patients With Cardiorespiratory Conditions Upon Hospital Discharge

Condition: Chronic Obstructive Lung Disease (COLD) · Heart Failure  ·  Sponsor: Corporació de Salut del Maresme i la Selva

PhaseNA
Planned participants200
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this randomized clinical trial is to determine whether an interdisciplinary, community-based intervention can reduce 30-day hospital readmissions and improve functional outcomes in patients aged 65 or older with chronic cardiac, respiratory, or mixed conditions following hospital discharge. The main questions it aims to answer are: Can the Reforça't program reduce 30-day hospital readmission rates to 25% compared to standard care? Does participation in Reforça't improve functional outcomes, medication adherence, quality of life, and mortality rates in this patient population? Researchers will compare patients enrolled in Reforça't (intervention group) with those receiving standard care (control group) to determine whether the program leads to lower readmission rates, improved health outcomes, and higher cost-effectiveness. Participants will: Undergo a pre- and post-intervention assessment (30 days post-discharge). Receive comprehensive, interdisciplinary care integrating medical, social, and rehabilitation services. Be monitored for 12 months to assess readmissions, survival, nursing home admissions, and overall well-being.

This description comes directly from the study's public registry record.

Talk to the study team

Griselda Manzano Monfort  ·  +34620215477  ·  gmanzano@salutms.cat

Noelia Quirant Arellano  ·  +34695803416  ·  nquirant@salutms.cat

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Comarcal de Calella - Corporació de Salut del Maresme i la SelvaCalella, Barcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06897410