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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
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

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Western Behavioral Health of the Alleghenies
Coordinator of this site? Confirm its status
AltoonaUnited StatesUnknown status
UPMC Western Behavioral Health at Safe Harbor
Coordinator of this site? Confirm its status
ErieUnited StatesUnknown status
Western Behavioral Health Mon Yough
Coordinator of this site? Confirm its status
McKeesportUnited StatesUnknown status
Comprehensive Recovery Services (Pittsburgh) of Western Psychiatric Hospital, Ambulatory Clinics and Residential Programs - UPMC, Pittsburgh, PA
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.