RecruitingNCT06286202
About this title
Integrative Neuro-social Cognitive Strategy Programme for Instilling REcovery (INSPIRE) a Community-Based Cognitive Remediation Trial
Read the official source — NCT06286202Official study titleIntegrative Neuro-social Cognitive Strategy Programme for Instilling REcovery (INSPIRE): a Community-Based Cognitive Remediation Trial
In SingaporeSchizophreniaBehavioural studyAges 21–60
- Countries
- Singapore
- Sponsor
- Singapore Institute of Technology
RecruitingNCT07085923
About this title
Norwegian Mental Illness Heart Health Study
Read the official source — NCT07085923Official study titleDietary Counselling And Exercise To Combat Cardiovascular Disease Risk In Norwegian Patients With A Severe Mental Illness
In OsloSchizophrenia, BipolarityBehavioural studyAges 25–70
- Countries
- Norway
- Sponsor
- Madeleine Elisabeth Angelsen
RecruitingNCT06005766
About this title
The Efficacy of Metacognitive Skills Training in the Context of Forensic Psychiatric Care
Read the official source — NCT06005766Official study titleDoes Group-Based Metacognitive Skills Training Reduce Jumping to Conclusions Bias of Patients With Psychotic Disorders in the Context of Forensic Psychiatric Care
In VaasaSchizophrenia, DepressionBehavioural studyAges 18+
- Countries
- Finland
- Sponsor
- University of Jyvaskyla
Not Yet RecruitingNCT07593456
Official study titleInvestigating a Gamified NegatIve-symptom Therapeutic Based on Evidence-based Cognitive Therapy (IGNITE)
This study isn't recruiting yet.
Multiple locations, including Glen OaksSchizophreniaDevice studyAges 18–65
- Countries
- United States
- Sponsor
- North Shore Therapeutics, Inc.
RecruitingNCT06650943
Official study titleEfficacy Study on Nursing Consultation in Weight and Metabolic Syndrome Management Based on the Carbohydrate-insulin Theory in Individuals with First-episode Psychosis (MetaKOP)
In BilbaoSchizophreniaBehavioural study
- Countries
- Spain
- Sponsor
- Hospital de Basurto
RecruitingNCT07387705
Official study titleOn Track for Wellness: Stepped-wedge Cluster Randomized Trial of a Fitbit Enhanced Health Intervention for Early Onset Psychosis
In ChicagoSchizophreniaInterventional study
- Countries
- United States
- Sponsor
- University of Illinois Chicago
CompletedNCT00650611
Official study titleA 27-Week Open-Label Trial To Characterize The Safety And Tolerability Of Orally Administered Ziprasidone In Children And Adolescent Subjects With Bipolar I Disorder (Manic Or Mixed), Schizophrenia Or Schizoaffective Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including San DiegoSchizophrenia, BipolarityMedication studyAges 10–17
- Countries
- United States
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
TerminatedNCT03669640
Official study titlePhase 2, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Effects of RO6889450 (Ralmitaront) in Patients With Schizophrenia or Schizoaffective Disorder and Negative Symptoms
This study ended early.
Multiple locations, including BellflowerSchizophreniaMedication studyAges 18–55
- Countries
- United States, Japan, Spain, + 1 other
- Sponsor
- Hoffmann-La Roche
WithdrawnNCT06878833
Official study titleA Multidose, Randomized, Double-Blind Study to Evaluate the Safety and Tolerability of Long-Acting Oral Risperidone (LYN-005) in Participants With Schizophrenia or Schizoaffective Disorder
This study was withdrawn before enrollment.
Location not clearly listedSchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Lyndra Inc.
CompletedNCT04512066
What is this study about?This study evaluated the safety and effectiveness of RO6889450 for people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18–45
- Countries
- United States, Japan, Russia, + 1 other
- Sponsor
- Hoffmann-La Roche
CompletedNCT01101464
Official study titleA Single-center, Open-label, 2-way Crossover Relative Bioavailability and Safety Trial With Two Differing Strength Tablets (3 x 5 mg vs. 1 x 15 mg) of Sublingually Administered Org 5222 in Subjects With Schizophrenia or Schizoaffective Disorder.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Organon and Co
CompletedNCT00306475
This study has finished and is no longer accepting participants.
In NashvilleSchizophreniaMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Northwestern University