Enriched Environment Program for Stroke Recovery

The Enriched Environment as an Integrated Tool in the Ward Setting

Recruiting N/A Interventional Study
Stroke Stroke, Acute
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
50 (estimated)
Sponsor
University of Padova · Other
Who this trial is looking for

This trial is looking for people who have had a stroke at least 24 hours ago. Participants will be involved in a program to help improve their well-being and recovery while in the hospital.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have had an ischemic or hemorrhagic stroke at least 24 hours ago.
  • I agree to participate in the study.
  • I am medically stable.

You may not be able to join if

  • I am uncooperative based on a cognitive assessment.
  • I am not medically stable or have a reduced level of consciousness.
  • I cannot maintain a sitting position or safe posture in a wheelchair.
  • I have difficulty understanding information due to speech issues.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The goal of this longitudinal interventional study is to integrate the enriched environment (EE) in the context of the Neurology Clinic ward of the General Hospital - University of Padua, by verifying its effectiveness and impact on psychological well-being, functional recovery, activity level, and quality of life in people with stroke.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Ischaemic or haemorrhagic stroke, in any territory, occurring at least 24 hours before enrollment; * Participant consent to participate in the study; * Mecial stabilisation. Exclusion Criteria: * Uncooperative participant, as assessed by theMontreal Cognitive Assessment scal…
Contacts

Francesca Venturini

049 8212341

ce.sperimentazione@aopd.veneto.it

CONTACT