NCT07043803Completed
Reduction of Anticholinergic Medications Among Persons With Schizophrenia or Other Psychiatric Disorders
Reduction of Anticholinergic Medications Project (RAMP) Among Persons With Schizophrenia or Other Psychiatric Disorders Across UPMC Behavioral Healthcare Partner Organizations Using a Stepped-wedge, Randomized Trial Study Design.
Source: ClinicalTrials.gov · Last updated 4 Jun 2026
Brief summary (registry, in English)
The goal of this study is to reduce Anticholinergic Medication (ACM) in persons with psychoses or serious mental illness, when these medications are no longer needed.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 53 (actual)
- First submitted
- 20 Jun 2025
- Start date
- 16 Jul 2025
- Primary completion date
- 31 May 2026
- Lead sponsor
- University of Pittsburgh
- Diseases
- Schizophrenia, Bipolar disorder
- NCT number
- NCT07043803
What you commit to
- Study type: Interventional
- Participants enrolled: 53
- From 16 Jul 2025 to the primary completion date, 31 May 2026
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- if the clinicians treating the potentially eligible patients consider them to be clinically unstable or if drug-addiction is the focus of treatment and participation in ACM de-prescription protocols is considered risky, the team will defer to the treating clinicians to exclude participants.
Other
- patients with ongoing Parkinsonian symptoms who require ACM meds for countering EPS side effects based on the Simpson-Angus Scale score cutoffs.
- The same exclusions will apply to those persons undergoing medical procedures and treatments that make participation in this ACM deprescription trial unwise per the treating team.
Who the study is looking for
- are 18 years or older
- have a chart DSM V diagnosis of schizophrenia spectrum or schizoaffective or bipolar disorder or any other mental illness disorder
- have received ACM and antipsychotic medications for 6 months or more
- are considered to be clinically stable (by the patient's healthcare team) for 3 months or more
- the ACM (e.g. benztropine and/or trihexyphenidyl) is being used to treat EPS associated with antipsychotic medications.
- on an examination using the modified Simpson-Angus Extrapyramidal Symptoms Scale (head dropping and leg pendulousness items are dropped), no single item rated at 3 or 4.
- able and willing to sign the approved informed consent document.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Western Behavioral Health of the Alleghenies Coordinator of this site? Confirm its status | Altoona | United States | Unknown status |
| UPMC Western Behavioral Health at Safe Harbor Coordinator of this site? Confirm its status | Erie | United States | Unknown status |
| Western Behavioral Health Mon Yough Coordinator of this site? Confirm its status | McKeesport | United States | Unknown status |
| Comprehensive Recovery Services (Pittsburgh) of Western Psychiatric Hospital, Ambulatory Clinics and Residential Programs - UPMC, Pittsburgh, PA Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.