Internet Based Intervention

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

Condition / disease
Location
Status: Not yet recruiting

Supporting Just-In-Time Consent for Prenatal Screening: The INFORM Study

This clinical trial is about prenatal genetic screening. It will test an intervention to help people make decisions about screening. The intervention is a short set of information cards about screening. This intervention is for pregnant participants. They will use the intervention on their mobile phone before they see their doctor. The study has one main question: * Do participants who use the intervention feel more confident when they make a decision about screening? Researchers will compare participants who use the intervention to participants who do not. All participants will have their usual care when they visit their doctor. What will participants do? * Participants must be pregnant. They will sign up for the study before their first doctor's visit for their pregnancy. This is the visit where their doctor usually talks with them about screening. * Some participants will use the intervention before their first doctor's visit. Other participants will not use it. * All participants will talk with a researcher on the phone after their first doctor's visit. * Participants who use the intervention will answer a short survey on their phone. * A few participants who use the intervention will talk with a researcher a second time on the phone.

Participants needed: 1,400
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Case Western Reserve UniversityUpdated: Jul 1, 2026Locations: 3
Eligibility criteria

Currently pregnant and receiving care at a participating collaborative site - Un... [+4]

Not pregnant, not a patient at a partner clinical site [+4]

Status: Recruiting

RCT: the Effectiveness of LifeHack in Improving Mental Wellbeing in University Students.

Psychological issues are common among university students and affect mental wellbeing. The Caring Universities (CU) project, involving nine Dutch universities, aims to enhance students' mental health through an annual online questionnaire and a platform offering guided eHealth interventions. One intervention, LifeHack, utilizes cognitive behavioral therapy-based modules to improve mental wellbeing by enhancing resilience and life skills. The effects of LifeHack with pre-post measurements (total n = 216 at post-test) found found that LifeHack led to improvements in mental wellbeing, but dropout rates were influenced by lack of motivation and module relevance. A personalized version of LifeHack is being developed to address these issues and will be evaluated in an RCT to assess its effectiveness in improving mental wellbeing and related outcomes among university students.

Participants needed: 217
Trial details
Age: 16-99Biological sex: AllType: InterventionalSponsor: Universiteit LeidenUpdated: Jun 22, 2025Locations: 2
Eligibility criteria

Being fluent in Dutch and/or English [+5]

Status: Not yet recruiting

Internet-delivered Cystic Fibrosis Mental Health Prevention, Wellness, Resource Program: How Does it Work?

The goal of the clinical trial is to test whether a mental health program that is delivered through the Internet works well for children and adolescents with cystic fibrosis (CF) and their healthy siblings. The main questions it aims to answer are: * Does the program improve the mental health such as depression and anxiety symptoms? * Does the program improve overall quality of life? * Does the program improve self-efficacy - an individual's belief in their ability to complete tasks to achieve their goals? Participants will: * Fill out an online survey asking questions about their personal and health information, as well as their mental health before the program * Complete the online mental health program * Fill out an online survey asking questions about their mental health after completing the program, and 1-month and 3-months following completing the program Participants be compared against another group of children with CF and their healthy siblings who are on a waitlist and receiving usual CF treatment. Researchers will compare participants scores before starting the program with their scores immediately following completing the program, 1-month, and 3-month after completing the program. Researchers hope to develop a program that improves mental health, quality of life, self-efficacy, and knowledge about CF.

Participants needed: 120
Trial details
Age: 8-12Biological sex: AllType: InterventionalSponsor: University of ReginaUpdated: Jun 10, 2025Locations: 2
Eligibility criteria

between the ages of 8 and 12 [+2]

have a severe cognitive impairment or a major comorbid medical or psychiatric il...

Status: Not yet recruiting

Feasibility Study: Self-guided iCBT for Mothers With Postpartum Depression.

The purpose of this study is to conduct a feasibility study to test the study procedure and a newly developed self-guided internet-based cognitive behavioral therapy program for mothers with postpartum depression.

Participants needed: 20
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of Southern DenmarkUpdated: Aug 30, 2024
Eligibility criteria

Edinburgh Postnatal Depression Scale (EPDS) score 11-18 [+2]

Thoughts of self-harm≥2 on EPDS item 10 [+5]