RECRUITING

Reduction of Anticholinergic Medications Among Persons With Schizophrenia or Other Psychiatric Disorders

Description

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.

Study Overview

Study Details

Study overview

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.

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.

Reduction of Anticholinergic Medications Among Persons With Schizophrenia or Other Psychiatric Disorders

Condition
Schizophenia Disorder
Intervention / Treatment

-

Contacts and Locations

Altoona

Western Behavioral Health of the Alleghenies, Altoona, Pennsylvania, United States, 16601

Erie

UPMC Western Behavioral Health at Safe Harbor, Erie, Pennsylvania, United States, 16508

McKeesport

Western Behavioral Health Mon Yough, McKeesport, Pennsylvania, United States, 16601

Pittsburgh

Comprehensive Recovery Services (Pittsburgh) of Western Psychiatric Hospital, Ambulatory Clinics and Residential Programs - UPMC, Pittsburgh, PA, Pittsburgh, Pennsylvania, United States, 15213

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. are 18 years or older
  • 2. have a chart DSM V diagnosis of schizophrenia spectrum or schizoaffective or bipolar disorder or any other mental illness disorder
  • 3. have received ACM and antipsychotic medications for 6 months or more
  • 4. are considered to be clinically stable (by the patient's healthcare team) for 3 months or more
  • 5. the ACM (e.g. benztropine and/or trihexyphenidyl) is being used to treat EPS associated with antipsychotic medications.
  • 6. 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.
  • 7. able and willing to sign the approved informed consent document.
  • 1. patients with ongoing Parkinsonian symptoms who require ACM meds for countering EPS side effects based on the Simpson-Angus Scale score cutoffs.
  • 2. 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.
  • 3. 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Pittsburgh,

Professor of Psychiatry, MD, PRINCIPAL_INVESTIGATOR, University of Pittsburgh

Study Record Dates

2026-05