Engagement, Patient

7

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

Condition / disease
Location
Status: Recruiting

NICU Utilization of Remote Voice Technology to Improve mateRnal Experience (NURTURE)

The study's objective is to conduct a Phase II randomized controlled trial examining the preliminary efficacy of the VoiceLove app compared to usual care on maternal postpartum depression in mothers with infants admitted to the Neonatal Intensive Care Unit (NICU). Primary aim: Assess the effects of VoiceLove on maternal postpartum depression, measured by the Edinburgh Postnatal Depression Scale (EPDS). The estimates from this study will be used for a future definitive Phase III trial. Secondary aim: Assess feasibility, acceptability, and patterns of communication and engagement among mothers, partners, and NICU clinicians during the NICU hospitalization, measured through app usage metrics, satisfaction surveys, and qualitative interviews. Additionally, we will evaluate effects of infant length of stay.

Participants needed: 150
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Vanderbilt University Medical CenterUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Admitted to the neonatal intensive care unit (NICU) [+11]

Infant [+13]

Status: Recruiting

Parents Helping Parents for Youth Vaping Cessation

The goal of this randomized controlled study is to test if this new intervention works to help adolescents quit vaping. A key feature of the program is the use of peer support for parents, delivered by trained parent coaches. Participants will complete baseline and follow up surveys. Parents in the intervention arm will receive peer support as part of the program.

Participants needed: 200
Trial details
Age: 15-18Biological sex: AllType: InterventionalSponsor: University of NebraskaUpdated: May 26, 2026Locations: 1
Eligibility criteria

15-18 [+6]

Status: Recruiting

QT-Digital Mental Health Engagement Study

Sexual and gender minority (SGM) populations are disproportionately impacted by mental health concerns relative to their heterosexual and cisgender peers. Despite high need, SGM populations continue to report unmet mental health needs because they cannot or do not access mental health services. Digital Mental Health (DMH) services have been recognized as feasible, economical, and effective options to broaden the availability of mental health care to consumers who face barriers to mental health help-seeking. SGM consumers cite a preference for DMH care and this delivery format holds promise to attend to major mental health care access barriers experienced by this consumer group. Yet, the availability of DMH services tailored to the needs of SGM consumers is limited, and a dearth of research examines SGM populations' actual engagement with DMH services. A potential solution to fully understand how SGM populations utilize DMH services would be to characterize their engagement within a natural setting. Leveraging an established partnership with Mental Health America (MHA), a non-profit mental health advocacy group offering free, evidence-based screenings and self-guided DMH resources, this study will follow a large, naturalistic sample of SGM DMH consumers with the aim to test tailored engagement strategies with SGM DMH consumers using a micro-randomized trial (MRT) design. Results of this study will inform if delivering engagement strategies can meaningfully increase initial and sustained engagement with MHA resources and which types of strategies, specifically, work best for which users.

Participants needed: 2,300
Trial details
Age: 14+Biological sex: AllType: InterventionalSponsor: University of WashingtonUpdated: May 8, 2026Locations: 2
Eligibility criteria

Users of the Mental Health America (MHA) website engaging from Internet Protocol... [+3]

IP addresses outside of the United States [+3]

Status: Recruiting

1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV

This study tests a 5-session cognitive behavioral approach program (herein referred to as the 1MoreStep intervention) to train Black women living with HIV (BWLWHI) and exposed to intimate partner violence (IPV) in the past 2 years (hereafter, BWLWHI) in: 1) cognitive and behavioral skills to access internal and external sources of strength (e.g. self-reliance, safety net); safety strategies, knowledge about Undetectable = Untransmissible (U=U) and HIV care; and reduce internalized and anticipated stigma; 2) communication skills to respond to enacted HIV and IPV stigma and enlist social support; and 3) addressing structural barriers to HIV care engagement with an HIV navigator component. The intervention is informed by the HIV-Stigma Framework and a resilient-reintegration model which views women as active participants in responding to IPV and managing life with HIV. Aim 1: Examine preliminary efficacy of the 1MoreStep intervention on: (a) IPV safety strategies (informal and formal resources, safety planning, and placating strategies at baseline, 3-month and 6-month follow-up visits); and (b) HIV care engagement (medical record confirmed visit with an HIV care provider, antiretroviral therapy (ART) prescription, medication adherence, and viral load status during 3-month and 6-month follow-up visits). Aim 2: Examine the acceptability and feasibility of the 1MoreStep intervention operationalized by (a) quantitative measures: session attendance and fidelity to key intervention components and (b) qualitative interviews to assess: program fit, facilitators and barriers to participation, and using 1MoreStep intervention skills.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Cis-gender female [+8]

Not a Cis-gender female [+8]

Status: Recruiting

Forge AHEAD: Feasibility of Yoga to Improve Cognitive Function

The investigators will conduct a two-phase pilot study to test the feasibility and acceptability of a 12-week Chair Yoga intervention for 20 heart-failure patients. Using a patient-centered approach, investigators will involve stakeholders in designing the protocol, gather patient feedback, and refine the protocol accordingly.

Participants needed: 20
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: Auburn UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Heart failure diagnosis [+1]

Traumatic brain injury, co-existing neurological and psychiatric disorders [+4]

Status: Recruiting

OTAGO Exercise Program and Motivational Interviewing

The goal of this study is to see if OTAGO instructors, who have been trained in a special communication method called motivational interviewing, can help older adults start and stick with the OTAGO exercise program. The results will help guide future research on how behavior change techniques can support other fall prevention strategies.

Participants needed: 60
Trial details
Age: 60-120Biological sex: AllType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Apr 16, 2025Locations: 1
Eligibility criteria

Age ≥60 [+5]

o Receiving ongoing physical therapy with a primary focus on improving balance a... [+5]

Status: Recruiting

Digital Navigators for Acceptance and Competence Development with Mental Health Apps

The goal of this clinical trial is to learn if and how so called "Digital Navigators" (DN) can help general practitioners, outpatient psychiatrists and psychologists as well as their treated patients to use digital mental health apps (DiGAs) and integrate it into their treatment. The main questions it aims to answer are: * What are the chances and implementation barriers of DN? * What are the acceptance and expectations towards DN? * Do DN affect the psychological health of patients? * Do DN affect the digital health literacy and technical competence of participants? Employees of medical teams (e.g. medical assistants) receive training to become a DN. Afterwards patients are accompanied and supported by the DN for 12 weeks to select and use a suitable app for their mental disorder.

Participants needed: 116
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medizinische Hochschule Brandenburg Theodor FontaneUpdated: Sep 3, 2024Locations: 6
Eligibility criteria

Main diagnosis according to ICD 10 F00-F69, F80-F99 [+4]

Acute danger to self or others [+3]