A Pharmaceutical Intervention to Reduce Drug-Related Problems in a Home Healthcare Program (NCT05820945) | Clinical Trial Compass
UnknownNot Applicable
A Pharmaceutical Intervention to Reduce Drug-Related Problems in a Home Healthcare Program
Spain432 participantsStarted 2020-03-02
Plain-language summary
The investigators' hypothesis is that the individualized review of the pharmacotherapeutic plans of patients in a home healthcare program will be effective in improving the quality and safety of treatments. This study aims to evaluate the effectiveness of a standardized pharmaceutical intervention for the review and optimization of pharmacological treatments in ATDOM patients (catalan home healthcare program at primary care level), compared to the usual management.
Who can participate
Age range
65 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.
Inclusion Criteria:
* Patient in the home care program
* Sixty-five years of age or older
* Active pharmacological treatment plan with at least one drug
Exclusion Criteria:
* The responsible physician considers that participation may harm the patient
Questions worth asking your doctor
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.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
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.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Medication-related problems
Timeframe: Baseline and 6 months follow-up
2
Medication related-problems per patient
Timeframe: Baseline and 6 months follow-up
3
Patients with one or more MRPs
Timeframe: Baseline and 6 months follow-up
4
Drugs per patient
Timeframe: Baseline and 6 months follow-up
5
Polymedicated patients
Timeframe: Baseline and 6 months follow-up
Trial details
NCT IDNCT05820945
SponsorFundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina