Experimental study to test the effectiveness of a psychoeducational intervention using virtual reality, aimed at caregivers of multi-pathological and polypharmacy persons to promote safer medication use at home. Experimental design with two groups (experimental and control), pre-post measures, and participants assignment to groups by simple randomization. Null hypothesis. There will be no differences in the frequency of medication errors at home, the severity of the consequences of medication errors, perceived self-efficacy, and health literacy between caregivers using a dosing device (control group) and caregivers using a dosing device with the reinforcement of a psychoeducational intervention designed ad hoc (experimental group).
Age range
18 Years – 85 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change from Baseline Frequency of Medication Errors after the intervention (6 months later).
Timeframe: Pre-intervention measure (6 months prior). Post-intervention measure (last 6 months).
Change from Baseline Health Literacy after the intervention (6 months later).
Timeframe: Pre- and post-intervention measurement (6 months time lapse).
Change from Baseline Therapeutic Adherence after the intervention (12 months later).
Timeframe: Pre- and post-intervention measurement (12 months time lapse).
Change from Baseline Locus of Control after the intervention (12 months later).
Timeframe: Pre- and post-intervention measurement (12 months time lapse).
Change from Baseline Self-efficacy after the intervention (12 months later).
Timeframe: Pre- and post-intervention measurement (12 months time lapse).
Perceived usefulness of the information provided at the time of intervention completion.
Timeframe: Post-intervention measure (15 days after the start of the intervention).
Perceived usefulness of the information provided after 3 months from the end of the intervention.
Timeframe: Post-intervention measure (after 3 months).
Perceived usefulness of the information provided after 6 months from the end of the intervention.
Timeframe: Post-intervention measure (after 6 months).
Perceived usefulness of the information provided after 12 months from the end of the intervention.
Timeframe: Post-intervention measure (after12 months).
Family Caregivers' Experience at the time of intervention completion.
Timeframe: Post-intervention measure (15 days after the start of the intervention).
Family Caregivers' Experience after 3 months from the end of the intervention.
Timeframe: Post-intervention measure (after 3 months).
Family Caregivers' Experience after 6 months from the end of the intervention.
Timeframe: Post-intervention measure (after 6 months).
Family Caregivers' Experience after 12 months from the end of the intervention.
Timeframe: Post-intervention measure (after 6 months).