Schizoaffective

3

Review clinical trials related to Schizoaffective. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Exercise-based Program for Rehabilitation of Veterans With Severe Mental Illness

This is a hybrid1, effectiveness-implementation study of yoga-based exercises (YE) as an adjunctive tool for rehabilitation among persons with Severe Mental Illness (SMI). The two-arm randomized controlled trial will compare the efficacy of YE compared to the Wellness Lifestyle Program (WLP). Primary outcomes of the study will be self-report and performance-based measures of community functioning, defined in the investigators study as social, leisure, employment, and life skills functioning in the community. Secondary outcomes will include cognition and physical fitness measures.

Participants needed: 112
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: VA Office of Research and DevelopmentUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Written informed consent; [+9]

Unable to provide written informed consent; [+11]

Status: Not yet recruiting

Frontal Gamma Coherence Neurofeedback for Patients With Schizophrenia

This preliminary, randomized, double-blind, placebo-controlled clinical trial will evaluate frontal gamma coherence neurofeedback in adults with schizophrenia. Thirty participants will be randomly assigned to receive either active neurofeedback or placebo neurofeedback using a study-provided mobile platform. Participants will complete baseline assessments in person at the University of California San Diego, receive training on home use of the neurofeedback platform, and complete twice-weekly 30-minute sessions at home for 12 weeks. Participants will return for midpoint and end-of-treatment assessments to evaluate feasibility, tolerability, cognitive outcomes, and neurophysiological target engagement.

Participants needed: 30
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: BioSignal Solutions LLCUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Voluntary informed consent to participate and capacity to consent as measured by... [+3]

Electroconvulsive therapy within six months of the baseline assessment; [+8]

Status: Recruiting

Does tDCS Change Synaptic Density in the Brains of Patients With Schizophrenia

This study will examine changes in synaptic density with transcranial direct current stimulation (tDCS) in the brains of patients with schizophrenia. Synaptic density levels will be measured using a novel positron emission tomography (PET) radiotracer \[18F\]SDM-8, which is currently the best-in-class method to quantify synaptic density in humans. This will be a companion study to a parent study by our group examining the effects of tDCS on treatment adherence in schizophrenia (REB #103-2018).

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre for Addiction and Mental HealthUpdated: Sep 23, 2025Locations: 1
Eligibility criteria

Male or female participants of any race or ethnicity [+4]

Unwilling or incapable to consent to the study based on the MacArthur Test of Co... [+14]