Skip to content

Impact of clinical pharmacist interventions on the clinical outcome of patients with Bipolar Disorder (BD)

Impact of clinical pharmacist interventions on the clinical outcome of patients with Bipolar Disorder (BD) in Roozbeh hospital

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210307050613N1
Enrollment
112
Registered
2021-08-21
Start date
2021-08-20
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder type 1. Bipolar Disorder

Interventions

Intervention 1: Intervention group: clinical pharmacist interventions and consultations during hospitalization then one month and three months after discharge as an outpatient. Intervention 2: Control

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients diagnosed with Bipolar Disorder type 1 based on DSM 5 criteria Patients older than 18 Taking at least one antipsychotic or mood stabilizer

Exclusion criteria

Exclusion criteria: Psychiatric comorbidities including Schizophrenia, Obsessive-Compulsive Disorder,Generalized anxiety Disorder, Panic Disorder Drug or disease induced bipolar disorder Substance abuse (other than nicotin or caffeine) since one year ago

Design outcomes

Primary

MeasureTime frame
Medication Appropriateness Index. Timepoint: During hospitalization, one month and three months after discharge. Method of measurement: Medication Appropriateness Index questionnaire.

Secondary

MeasureTime frame
Depression score. Timepoint: During hospitalization, one months and three months after discharge. Method of measurement: Beck Depression Inventory questionnaire.;WHOQOL-BREF (WHO Quality Of Life). Timepoint: During hospitalization, one month and three months after discharge. Method of measurement: WHO Quality Of Life questionnaire.;Adherence to treatment plan. Timepoint: During hospital stay, one month and three months after discharge. Method of measurement: Medication Adherence Rating Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNazanin Gorgzadeh

Tehran University of Medical Sciences

nazanin.gz67@gmail.com+98 21 4436 3885

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026