Clinical trials

5

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

Condition / disease
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Status: Not yet recruiting

Informing Patients About Their Surgery's Environmental Impact: an Effective Pathway to Sustainable Healthcare?

The healthcare sector contributes significantly to climate change. Reducing the number of patients receiving resource-intensive procedures such as surgery can lower carbon emissions, particularly when two treatments with comparable clinical outcomes are available. Nevertheless, the impact of incorporating environmental considerations into patients' decision-making processes remains underexplored. The investigators examine how including information about the environmental impact of treatment options in a gallstone decision aid affects patients' real-life choice between surgery and the more sustainable alternative of conservative treatment. Moreover, the investigators examine whether factors such as severity of symptoms moderate the relation between sustainability information and patients' treatment choice. An exploratory vignette study informed the hypotheses that will be tested among actual patients with gallstones making actual treatment decisions. The results of this ecologically valid study have implications for both clinical practice and healthcare policy by offering insight into the effectiveness of pathways to include patients in the transition towards sustainable healthcare.

Participants needed: 400
Trial details
Biological sex: AllType: InterventionalSponsor: University of AmsterdamUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Patients who were referred to three participating hospitals located across the N... [+1]

None

Status: Recruiting

Imagery Rescripting in Primary Care

In the current study we aim to investigate the feasibility, acceptability, and effectiveness of ImRs offered by mental health assistants within primary care to reduce depressive symptoms. In a single-case experimental design (SCED) study, the following hypotheses will be tested: 1. ImRs results in a reduction of depressive symptoms compared to baseline, and this reduction lasts up to six months. 2. Patients with complaints of depressive symptoms find ImRs an acceptable form of intervention when offered by mental health assistants within a general practice setting. Participants will wait for 2-4 weeks and then receive 5 sessions of ImRs over a period of 10 weeks. During these sessions, negative memories related to their depressed feelings are rescripted.

Participants needed: 12
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of AmsterdamUpdated: Jan 23, 2026Locations: 1
Eligibility criteria

Main complaint of depressive feelings, as indicated by both the mental health as... [+4]

Acute suicide risk (BDI-II-item9 score of 3). [+1]

Status: Recruiting

Hold me Tight/Let me Go: Effectiveness of a Course to Enhance Parent-adolescent Relationship

HmT/LmG is a group course for 4-6 parental dyads and consists of 4 group sessions with psycho-education and skills training and 3 individual sessions per family (i.e., 1 session with the adolescent, 1 session with the parents, and 1 session with parents and adolescent together). We want to evaluate effectiveness and treatment process mechanisms applying self-reports, audio observation and interviews.

Participants needed: 150
Trial details
Age: 12-18Biological sex: AllType: ObservationalSponsor: University of AmsterdamUpdated: Dec 24, 2025Locations: 5
Eligibility criteria

Families with one or both parents/primary caretaker (single parent or blended fa... [+4]

Status: Not yet recruiting

Imagery Rescripting for Pathological Affective Dependence and Intimate Partner Violence

The goal of this multiple baseline case series study is to evaluate the effectiveness of Imagery Rescripting for Pathological Affective Dependence (PAD) in victims of Intimate Partner Violence (IPV). The primary research questions are: Does Imagery Rescripting reduce PAD and/or commitment to the abusive relationship after separation? Does Imagery Rescripting also reduce traumatic symptoms? Does Imagery Rescripting improve general mental health, self-compassion, and resilience in IPV victims? Participants will undergo a waiting period of 5-9 weeks (to assess time effects without treatment), followed by 4 weekly preparation sessions, 12 weekly Imagery Rescripting sessions, and 1 month of post-treatment. Throughout the study, participants will rate the severity of PAD and relational commitment on a weekly basis. They will also complete more detailed questionnaires assessing mental health, traumatic symptoms, resilience, and self-compassion before each phase, at 1 month post-treatment, 3 months post-treatment, and during follow-ups at 6 and 12 months.

Participants needed: 18
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: University of AmsterdamUpdated: Nov 1, 2024Locations: 3
Eligibility criteria

Experience of IPV (from a clinical interview) [+1]

Comorbidity with the following diagnoses: psychosis, schizophrenia, bipolar diso... [+8]

Status: Recruiting

MOTIV8 - Treatment Motivation in Forensic Youth Treatment

This project entails to gain a deeper understanding of the development of treatment motivation over the course of intramural and outpatient forensic youth care. Research questions are 1) How does treatment motivation of youth and parents develop over the course of forensic systemic therapy, and following the transition from inpatient to outpatient therapy?; 2) Which client factors, interpersonal factors, and contextual characteristics moderate the development of treatment motivation?; 3) Which mechanisms play a role in the development of treatment motivation?; and 4) How does treatment motivation affect treatment retention and the achievement of primary therapy goals?

Participants needed: 16
Trial details
Age: 12-24Biological sex: MaleType: ObservationalSponsor: University of AmsterdamUpdated: Jun 25, 2024Locations: 1Duration: 9 Months
Eligibility criteria

Not listed