Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Transcutaneous Auricular Neurostimulation (tAN) for Premenstrual Dysphoric Disorder (PMDD) and Perimenopause

Transcutaneous Auricular Neurostimulation (tAN) will be administered to women with premenstrual syndrome (PMS), premenstrual dysphoric disorder (PMDD), and perimenopause. The investigators will examine whether tAN improves symptomology by collecting self-report data before the intervention, during the intervention, and following the intervention.

Participants needed: 20
Trial details
Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Texas Christian UniversityUpdated: Jul 7, 2026Locations: 1
Eligibility criteria

Assigned female at birth [+5]

Using hormonal birth control [+33]

Status: Not yet recruiting

Justice Community Overdose Innovation Network II TCU Hub

The current study proposes to use a Hybrid Type 3 implementation research strategy to: 1) Significantly enhance our understanding of public health outcomes \[e.g., overdose incidents and substance-use (SU)-related Emergency Medical Service (EMS) contacts\] and public safety outcomes (e.g., drug-related arrests) associated with Deflection and Pre-Arrest Diversion initiatives (DPAD, hereafter referred to as Deflection); and 2) Create a lasting contribution to the fields of research focused on SU and the criminal legal system (CLS) by advancing knowledge of effective implementation strategies involving the critical role of community engagement in Deflection. The highly experienced team of Multiple PIs, senior-level collaborators from both Deflection and Community Behavioral Health (CBH), state-level evaluation partners, a national stakeholder advisory group, and CLS and behavioral health partners within each community have teamed up to carry out the proposed project. The study approach uses a hybrid implementation-effectiveness design to examine strategies to improve opioid and stimulant relevant outcomes, and specifically proposes to test the implementation-effectiveness of 2 strategy bundles to promote Deflection models through a CORE community engagement bundle (designed to facilitate community stakeholder engagement) and ENHANCED community engagement bundle (CORE plus a component to systematically involve community advocates) on improving implementation as well as public safety and health outcomes. The proposed randomized control trial includes a total of 20 geographically distinct clinical research performance sites (i.e., 20 communities spanning 5 states; New Mexico, Illinois, Wisconsin, Colorado, and Pennsylvania), with 3-5 communities per state and the inclusion of key CLS and CBH stakeholders within each site. The large scope of the project will maximize potential generalizability of study results and sustainability of implementation strategies.

Participants needed: 1,620
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Texas Christian UniversityUpdated: Apr 14, 2026Locations: 1
Eligibility criteria

Making referrals (e.g., law enforcement, first responders, community agencies) &... [+3]

Not affiliated with a participating Deflection agency; [+31]

Status: Recruiting

Exploration of an Online Education Program to Support Caregivers' Knowledge Transfer

The overarching goal of this work is to determine methods that improve caregiver education about the behavioral and psychological symptoms (BPSD) of dementia. The specific goal of this project is to extend our prior work to evaluate the impact of our educational intervention on caregivers' ability to transfer knowledge about the management of ADRD to real-world applied examples.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Texas Christian UniversityUpdated: Jan 29, 2026Locations: 2
Eligibility criteria

informal caregivers [+4]

professional caregivers [+2]

Status: Recruiting

Translaryngeal Vibration for Hyperfunctional Voice Disorders

Contemporary treatments for hyperfunctional voice disorders such as muscle tension dysphonia (MTD) are effective but typically do not restore voice handicap or voice function to normal thresholds. Recent reports of vibration as a voice therapy modality have been published, but many questions remain about the efficacy of this tool. The current project addresses these problems through a blinded and randomized controlled trial to investigate the efficacy of local translaryngeal vibration for MTD and the dose-response relationship of this modality when compared to treatment without vibration.

Participants needed: 30
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Texas Christian UniversityUpdated: Aug 28, 2025Locations: 1
Eligibility criteria

a) diagnosis by an otolaryngologist of hyperfunctional dysphonia (MTD) without b...

Unable to receive vibration to neck area