Clinical trials

11

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Condition / disease
Location
Status: Recruiting

An Ecological Momentary Intervention for the Reduction of Impairment in Somatic Symptom Disorder

Persistent somatic symptoms significantly impair the daily lives of individuals with Somatic Symptom Disorder (SSD). Negative psychological factors (NPFs), such as catastrophizing and negative affectivity, further compound this impairment. Yet, few studies have examined strategies in daily life that directly target somatic symptoms and their dynamic relationship with NPFs. The goal of this clinical trial is to investigate if an Ecological Momentary Intervention (EMI) using music listening and cognitive reappraisal can reduce the intensity of and impairment due to somatic symptoms in 40 individuals with Somatic Symptom Disorder (SSD), aged 18-65 years. Participants will report symptom intensity, impairment, and NPFs up to four times daily via a smartphone app over a six-week period. Using an intraindividual randomized controlled design, during weeks two to five, participants will be randomly assigned in the ratio of 50:25:25 to no intervention, music listening, and cognitive reappraisal, both at fixed times (evening measurement) and during episodes of acute somatic impairment.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Jun 12, 2026Locations: 1
Eligibility criteria

Somatic Symptom Disorder

chronic physical illnesses that fully explain the somatic symptoms [+6]

Status: Recruiting

Nitrate, Exercise and Vascular Function in Midlife Women

The purpose of this clinical study in women after menopause is to investigate whether the daily intake of nitrate from beetroot juice over 12 weeks enhances the positive effect of exercise training on vascular function, blood pressure and physical performance. The risk of cardiovascular diseases (CVD) increases with advancing age and women are particularly affected. In women, the decline in the sex hormone oestrogen in the blood circulation with menopause contributes to impaired vascular function and an increased CVD risk; in part through increased inflammatory processes, oxidative stress, and a reduced body's own production of nitric oxide (NO). NO is a signaling molecule that is important for vascular function. Endurance-based exercise training is a key lifestyle strategy to prevent CVD. However, studies indicate that exercise is less effective in terms of its health-promoting adaptations in women after menopause as compared with men of similar age. This study investigates the effect of exercise training in combination with the intake of nitrate-rich beetroot juice on functions of the cardiovascular system. Nitrate is a nitrogen compound that is found naturally in plant foods (e.g. beetroot juice) and is converted to NO in the human body. Results of previous studies indicate vasodilatory, blood pressure-lowering and performance-enhancing effects as well as positive influences on inflammatory processes and oxidative stress following nitrate intake. The hypothesis is that nitrate intake concomitant to training promotes training adaptations and further improves vascular function, blood pressure and physical performance compared to training without nitrate intake. For the study, 54 untrained postmenopausal women (with the ages between 45 and 65 years) will be recruited and randomly allocated into two groups. Both groups will undergo 12 weeks of endurance-based exercise training. One group will receive nitrate-rich beetroot juice, and the other nitrate-depleted beetroot juice (as placebo). Vascular function, blood pressure, maximum oxygen uptake, and blood biomarkers for nitrate metabolism, inflammation status and oxidative stress will be examined. The anticipated study results will provide new insights into whether nitrate as a 'training adjunct' improves health-promoting training adaptations in women after menopause. The overall aim is to improve the cardiovascular health and performance of middle-aged women and reduce their increased CVD risk.

Participants needed: 54
Trial details
Age: 45-65Biological sex: FemaleType: InterventionalSponsor: University of ViennaUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Postmenopausal women (amenorrhoeic ≥1 year), between the ages of 45 and 65 years... [+1]

Current or recent (within previous 3 months) engagement in exercise training (i.... [+18]

Status: Recruiting

Collagen Peptides and Cellular Aging

The goal of this clinical trial is to learn if daily collagen peptide supplementation can stabilize or lengthen telomeres and improve related markers of cellular aging in adults aged 50-70 years with overweight and low-to-moderate physical activity (healthy volunteers without major chronic disease). Main questions it aims to answer are: Does six months of collagen peptides stabilize or extend telomere length and increase telomerase activity compared with placebo? Are any telomere-related changes associated with lower inflammation, healthier body composition, and better functional health? Researchers will compare collagen as an intervention to a placebo group to see if collagen will influence aging markers. Participants will take collagen peptides or a placebo daily for 24 weeks. They will attend three study visits: one before starting the intervention (T0), one at 3 months (T1), and one at 6 months (T2). At each visit, blood samples will be collected to measure telomere length, telomerase activity, and inflammation/redox markers. Participants will also undergo body composition assessments using bioelectrical impedance, complete functional tests of muscle strength and mobility, and fill out questionnaires on health and vitality.

Participants needed: 125
Trial details
Age: 50-70Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: May 5, 2026Locations: 1
Eligibility criteria

Adults aged 50-70 years; both male and female participants are eligible [+5]

Diagnosed chronic diseases relevant to the immune system, metabolism, or cellula... [+5]

Status: Recruiting

L-serine and Strength Training in the Elderly

This study investigates whether taking the amino acid L-serine, either alone or in combination with targeted strength training, can have a positive effect on mental performance, brain function, and physical fitness in older people. Healthy, independent women and men aged 65 to 85 are eligible to participate. Participants will be randomly assigned to one of three groups: placebo, L-serine, or L-serine combined with strength training. Cognitive tests, physical performance tests, and blood and brain tests will be conducted over a period of 48 weeks. The aim is to gain a better understanding of how nutrition and exercise can contribute to healthy aging.

Participants needed: 126
Trial details
Age: 65-85Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Men and women between the ages of 65 and 85 [+2]

Chronic diseases that contraindicate medical training therapy [+6]

Status: Recruiting

Discrimination of N2a and N2b by EBUS-TBNA: is a Change of the Needle Necessary?

During EBUS staging in patients with mediastinal lymphadenopathy, it is planned to perform a first round of staging with change of the needle between all lymph nodes and a second round of staging without change of the needle.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Feb 18, 2026Locations: 1
Eligibility criteria

Pulmonary lesion suspicious for lung cancer or histologically confirmed lung can... [+1]

Status: Recruiting

Night Shift Work and Biomarkers of Obesity Risk in Hospital and Industry Workers

Shift work is a well-known risk factor for the development of overweight and obesity, which may lead to downstream effects such as increased risk of cardiometabolic diseases and cancer. However, the biological and behavioral mechanisms underlying the obesogenicity of night shift work are not well understood. Population-based mechanistic studies in real life shift workers are needed to address how night shift work impacts metabolic health. The investigators aim to characterize the behavioural, environmental, and biological mechanisms and pathways for the association of night shift work and obesity across Europe. The investigators will conduct a cross sectional study in 5 European countries (Austria, Denmark, Germany, Netherlands and Poland) and recruit 1000 rotating night shift workers and day workers (200/country) from the health sector and different industries. Night and day workers will be age-frequency (3 age groups), gender and (where possible) working tasks matched. Participants will complete online questionnaires and report their diet habits in a mobile app. Body composition, dietary behavior and sensory preferences will be tested. Biologic specimens (blood, urine, saliva, hair and feces) will be collected at the workplace on a day where participants are working on a day shift (or a day off). In a subsample (Austria and Netherlands) shift workers will provide biological samples (spot blood, urine and saliva) both on a day shift and on a night shift. Biomarkers including hormones, cellular immunity and inflammation, parameters linked to gut health and metabolism of fat and sugar, appetite, oxidative stress, metabolomics and microbiota will be measured. The investigators hypothesize that compared to day workers, night shift workers will experience disrupted levels of pre-obesity markers. Higher circadian disruption, sleep disruption and mistimed eating patterns workers will be associated with more disrupted biomarker profiles. Among rotating shift workers, night shift will be associated with acute disrupted melatonin production, metabolomic profiles and composition of oral microbiota compared to a day shift.

Participants needed: 1,000
Trial details
Age: 21+Biological sex: AllType: ObservationalSponsor: University of ViennaUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Health care sector or industrial shift worker [+11]

Pregnancy [+7]

Status: Recruiting

Hop Compounds on the Immune System in Overweight People

The aim of the present study is to determine the effect of Iso-alpha Acids and Xanthohumol from hops on the immune response in overweight participants.

Participants needed: 24
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Apr 15, 2025Locations: 1
Eligibility criteria

BMI 25 - 29,9 kg/m² [+3]

History of diseases that could falsify the study results [+9]

Status: Recruiting

Xanthohumol and Viral Infections (XL)

The aim of the present study is to determine if a regular oral supplementation of xanthohumol attenuate the severity of symptoms and duration of´viral infections.

Participants needed: 100
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Apr 15, 2025Locations: 1
Eligibility criteria

healthy [+1]

food intolerances [+7]

Status: Recruiting

Hop Compounds on the Immune System (VH)

The aim of the present study is to determine the effect of Iso-alpha-Acids and Xanthohumol from hops on the immune response of healthy participants over a timeframe of 6 hours.

Participants needed: 14
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Apr 15, 2025Locations: 1
Eligibility criteria

healthy [+1]

food intolerances [+5]

Status: Recruiting

PRObing The Efficacy of Commercial Stage Storage Buffers and Evaluating Gut Metaproteome Variability Between Individuals

The study aims to assess the effectiveness of various commercial and non-hazardous buffers for the storage of human gut fecal samples over time. This evaluation will be conducted by comparing the performance of these buffers against directly frozen samples using metaproteomic analysis. The study is motivated by the need for standardized protocols for sample preservation in metaproteomic research, particularly focusing on protein preservation in fecal samples. By investigating proteomic, taxonomic, and functional identifications, the research seeks to provide insights into the reliability of these buffers as storage solutions. Additionally, the study plans to explore inter- and intra-individual variabilities at the proteome level by periodically collecting fecal samples from volunteers, complementing existing knowledge in metaproteomics. Overall, the study addresses a critical gap in the field and has the potential to enhance reproducibility and comparability across metaproteomic studies

Participants needed: 52
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: University of ViennaUpdated: Mar 25, 2025Locations: 1
Eligibility criteria

agreeing to participate after signing the informed consent form and [+1]

take antibiotics during the previous 1 month [+1]

Status: Not yet recruiting

Youth Mental Health Recovery in the Family After Inpatient Stay

The goal of this longitudinal mixed-methods study is to investigate caregiver strain, family processes and health outcomes after youth psychiatric inpatient treatment. Caregivers of youth who received inpatient treatment for mental health problems will complete a survey at three timepoints (baseline, 3- and 6- month followup) reporting on youth outcomes, caregiver well-being, and family processes. Qualitative interviews on caregivers' challenges, needs, and resources around the return to home care are conducted with a subsample (target n = 10) of participants. The main research questions (RQs) are: RQ 1: Do family processes contribute to youth mental health outcomes after discharge from inpatient treatment? RQ 1a: What family-level risk factors predict youth readmission to inpatient treatment? RQ 1b: Do family processes predict youth mental health trajectories over time? RQ 2: Is there a reciprocal relationship between youth mental health problems and caregiver burden? RQ 2a: Do family processes mediate the association between caregiver burden and youth mental health problems? RQ 3: How do caregivers experience their children's return to home care? RQ 3a: What challenges and needs do caregivers report? RQ 3b: What types of follow-up services do families receive and/or have access to? RQ 3c: How do caregivers cope with ongoing difficulties in the post-discharge period?

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of ViennaUpdated: Mar 17, 2025
Eligibility criteria

18 years or older [+2]

another caregiver of the same child has already participated in the study [+1]