Schizoaffective

2

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

Condition / disease
Location
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: Sep 24, 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

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]