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NCT ID: NCT04655196 Completed - Loneliness Clinical Trials

Evaluation of the Efficacy of Two Internet-based Self-help Interventions for Loneliness.

SOLUS-D
Start date: May 17, 2021
Phase: N/A
Study type: Interventional

In this study, people who suffer from loneliness will be randomized to three study conditions. The first and second group get an account to an internet-based self-help intervention. The first group also receives weekly feedback from a coach and the second group receives an automated email on a weekly basis. The third group is a waiting control group. In all three conditions additional care or treatment is allowed. The aim of the study is to investigate the efficacy of an internet-based self-help intervention to reduce feelings of loneliness compared to a waiting list and the effect of support during the intervention. Assessments are at baseline, 5-week, 10-week, 6-months and 12-months post-randomization. Participants in the waiting control group get also access to the intervention and fill out questionnaires at baseline, 5-week and 10-week post-randomization and get also access to the intervention 10 weeks after randomization.

NCT ID: NCT04652557 Completed - Working Memory Clinical Trials

Influence of Fampridine on Working Memory in Healthy Young Subjects

FamH
Start date: November 1, 2021
Phase: Phase 2
Study type: Interventional

Proof of concept study on the acute effects on working memory of 10 mg fampridine SR as well as the effects after repeated administration of 10 mg twice daily (3.5 days). The hypothesis ist that fampridine improves working memory performance.

NCT ID: NCT04652544 Completed - Clinical trials for Spinal Cord Injuries

Vitamin D Supplementation in Individuals With a Chronic Spinal Cord Injury

Start date: May 19, 2021
Phase: Phase 3
Study type: Interventional

The main objective of this placebo-controlled randomized double-blinded study is to investigate the effect of vitamin D supplementation on vitamin D status (25(OH)D concentration in the blood) among individuals with a chronic spinal cord injury (SCI). Further, the effects of vitamin D supplementation on several other parameters (e.g. bone density and mood) are investigated, which could reveal positive secondary effects of supplementation that are especially relevant for clinical practice.

NCT ID: NCT04650776 Completed - Heat Stress Clinical Trials

Non-invasive Prediction of Thermal Strain in Healthy Male Adults

HUMONHEAT
Start date: September 1, 2017
Phase: N/A
Study type: Interventional

This is primarily an experimental study investigating methods of temperature measurement / heat strain detection. In the calibration study, there are different skin temperature sensor types, and in the prediction study there are different methods for determining heat strain, including conventional methods (rectal, gastro-intestinal), the development of a prediction model, and an index based on heart rate variability.

NCT ID: NCT04648137 Completed - Diabetes Insipidus Clinical Trials

Circulating Oxytocin Changes in Response to the Oxytocin System Stimulator MDMA in Patients With Diabetes Insipidus and Healthy Controls

OxyMA
Start date: February 5, 2021
Phase: N/A
Study type: Interventional

This study is to evaluate oxytocin levels in response to MDMA administration as compared to placebo in patients with diabetes insipidus and healthy volunteers.

NCT ID: NCT04647500 Completed - Clinical trials for 22q11.2 Deletion Syndrome

Effects of Methylphenidate on Brain and Cognition in 22q11 Deletion Syndrome

Start date: August 26, 2016
Phase: N/A
Study type: Interventional

Chromosome 22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated with a high risk of psychiatric disorders, including schizophrenia spectrum disorders. This population is characterized by a specific neurocognitive profile and atypical brain development. Methylphenidate is a psychostimulant used in the treatment of attention deficit with/without hyperactivity (ADHD). Although ADHD is one of the most important co-morbidities in 22q11DS, affecting 35-45% of patients, to date only two studies have focused on quantifying the efficacy of this treatment in this population. The objective of this study is to quantify the improvement in cognitive performance as well as the differences in brain connectivity associated with the methylphenidate molecule in a population at risk of cognitive impairment and the development of schizophrenia.

NCT ID: NCT04645654 Completed - Postoperative Pain Clinical Trials

Brief Postoperative Hypnosis Intervention as Multimodal Analgesia After Major Abdominal Surgery

Hypn+ERAS
Start date: October 1, 2020
Phase: N/A
Study type: Interventional

This study will measure the efficacy of hypnosis on pain after a major abdominal surgery. The aim is to further improve comfort and rehabilitation of patients after surgery, beyond the usual early recovery after surgery (ERAS) enhancement protocols. Patients will be randomised (1:2) to the standard of care regarding pain management and rehabilitation, as part of the ERAS protocol, vs. ERAS + an additional hypnosis intervention. In this group, hospitalised patients are given 3 hypnosis sessions targeting analgesia between postoperative day 1 to 12. The study will collect outcomes about pain and its burden, sleep quality, appetite, mobilisation and mood. Secondary outcomes also include use of pain medication and length of hospital stay.

NCT ID: NCT04644978 Completed - Mental Illness Clinical Trials

European Study on the Attitude of Psychiatrists Towards Their Patients

Eustigma
Start date: July 29, 2020
Phase:
Study type: Observational

Background: Many people think that people with mental disorders might be dangerous or unpredictable. These patients face various sources of disadvantages and experience discrimination on job interviews, in education, and housing. Mental health-related stigma (MHS) occurs not only within the public community, it is a growing issue among professionals as well. Aim: The investigators designed a prospective, observational, multi-centre, international study of 35 European countries to investigate the MHS among medical specialists and trainees in the field of general adult and child and adolescent psychiatry. Methods: An internet-based, anonymous survey will measure the stigmatizing attitude by using the local version of the Opening Minds Stigma Scale for Health Care Providers. Presentation of the Results: The results of the research will be published in an international peer-reviewed journal. Furthermore, the research team will present the results at national and international conferences.

NCT ID: NCT04643340 Completed - Healthy Clinical Trials

Imaging During Subliminal Perception

Start date: March 15, 2020
Phase:
Study type: Observational

Subliminal perception of visual stimuli can be studied with functional brain imaging, e.g. with functional magnetic resonance imaging (fMRI). However, it is unclear how subliminal perception affects connectivity in the brain. Further, it is not known if real-time (rt) fMRI neurofeedback of brain areas involved in subliminal perception can lead to supra-threshold perception. For attention tasks, the investigators hypothesize that functional connectivity strength is mediated by the insular cortex during both supra-threshold and subliminal perception. Additionally, the investigators hypothesize that rt-fMRI neurofeedback training should alter neuronal and behavioral responses.

NCT ID: NCT04642781 Completed - Healthy Children Clinical Trials

Measurement of Eye Movements While Reading a German Text

Start date: March 30, 2018
Phase:
Study type: Observational

To establish normative value for reading parameters in healthy children of primary school age and in grades 2-5.