Prevention Intervention

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

Condition / disease
Location
Status: Recruiting

Prevent Language Delays and Disorders Among Children of Caregivers With Substance Use Disorders With Community Groups and Individualized Services

The goal of this clinical trial is to test ways to improve early language development among young children of parents with substance use disorder (SUD). Children of parents with SUD are at increased risk for language delays, and early supports may help prevent long-term learning challenges. This study will examine whether adding additional supports to group-based parenting intervention improves child language outcomes compared to the group intervention alone.

Participants needed: 244
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of OregonUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

Self-reported lifetime history of substance use disorder treatment and/or [+11]

Status: Recruiting

Healthy Older Adults Through Movement and Engagement

The HOME Project evaluates the effects of structured health dialogues with individuals aged 67-84 years in the municipality of Borgholm, Sweden. A combination of registry data and survey responses will be used to monitor quality of life, morbidity, healthcare needs, and lifestyle factors over a six-year period. Outcomes will be compared between randomized groups within Borgholm municipality and a matched control group from seven other municipalities in Region Kalmar. The project also includes an analysis of cost-effectiveness and the reach of the intervention. A qualitative interview study will explore participants' perceptions of their health, their motivations for health improvement, and their experiences of how the health dialogues may influence these aspects. In a substudy, machine learning models will be developed to predict functional decline and high healthcare needs among older adults. These models will be validated against established risk assessment tools such as the Adjusted Clinical Groups (ACG) system and the Charlson Comorbidity Index. Digital motion analysis using Skeleton Avatar Technology will be employed both independently and in combination with other variables to support model development.

Participants needed: 2,952
Trial details
Age: 67-84Biological sex: AllType: InterventionalSponsor: Linkoeping UniversityUpdated: Oct 7, 2025Locations: 1
Eligibility criteria

Living in Borgholm municipality or in one of 7 matched Demographical Statistical... [+1]

Living in a nursing home [+1]

Status: Not yet recruiting

Implementing Online Mental Health Program

This study evaluates the feasibility, acceptability, and sustainability of MINDxYOU, a self-guided online psychotherapy program designed to reduce stress and improve the mental well-being of healthcare professionals in the Andalusian public health system. The trial uses a hybrid type 3 effectiveness-implementation design, combining the evaluation of implementation outcomes with observation of clinical effects on stress, anxiety, and depression. The intervention includes mindfulness, compassion, and acceptance-based practices delivered in four online modules over eight weeks. The study will be conducted in two phases: an initial hospital-based pilot and a broader rollout across primary care and hospital centers. Results will help identify how digital mental health interventions can be integrated into routine healthcare settings to support professionals working under high stress.

Participants needed: 130
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y SaludUpdated: Jul 15, 2025Locations: 1
Eligibility criteria

Being a current healthcare professional. [+4]

Diagnosis of serious mental illness. [+2]

Status: Recruiting

Talking for Change: Secondary Prevention of Child Sexual Abuse Perpetration

The goal of this patient preference randomized controlled trial is to investigate the efficacy of Talking for Change (TFC), an intervention for the secondary prevention of child sexual abuse and exploitation (CSA) perpetration. Blinded clinical raters will evaluate the primary endpoint-reductions in dynamic risk factors for sexual offending against children-and clients will provide self-reports to evaluate a second primary outcome-reductions in sexual contact with children, accessing online child sexual exploitation material (CSEM), and desire for sexual contact with children. Researchers will compare the following groups: (1) those receiving 20 weeks of the experimental TFC group psychotherapy; (2) those receiving 20 weeks of a control group psychotherapy targeting mental health and stress more broadly; and (3) those receiving no treatment.

Participants needed: 220
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Centre for Addiction and Mental HealthUpdated: Jun 12, 2025Locations: 1
Eligibility criteria

Must be deemed to have capacity to provide informed consent; [+9]

Inability to engage meaningfully in group psychotherapy (e.g., due to intellectu... [+2]