Lifestyle Factors

13

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

Condition / disease
Location
Status: Recruiting

A Digital Lifestyle Intervention in Primary Healthcare to Prevent Cardiovascular Disease

Unhealthy lifestyle behaviors are well-established risk factors for cardiovascular disease (CVD) which is the leading cause of death globally and in Sweden. Digitalization offers new and better possibilities for healthcare to fulfil their responsibility to support healthier lifestyles, however, to ensure scalability and sustained implementation of digital tools within healthcare, digital interventions need to be systematically maintained and delivered by the primary healthcare. The aim of this project is to evaluate whether a digital lifestyle intervention, developed within Swedish primary healthcare, can improve clinically important cardiovascular health outcomes and lifestyle behaviors. In this multi-center randomized controlled trial patients, 40-60 years, in Swedish primary healthcare will be recruited and randomized to the control or intervention group. All participants will receive standard care consisting of one structured health dialogue focused on lifestyle habits. The intervention group will also receive support through the digital lifestyle intervention for creating healthy habits regarding diet, physical activity, alcohol consumption, and tobacco usage. The primary outcome is LDL-cholesterol at 6 months post-randomization. Secondary outcomes 6 months post-randomization are HDL-, total cholesterol, fasting blood glucose, triglycerides, non-HDL, blood pressure, weight, height, BMI, waist circumference, cardiovascular risk evaluation (SCORE2), dietary intake, physical activity, sleep, stress, alcohol consumption, tobacco use, and health-related quality of life.

Participants needed: 1,000
Trial details
Age: 39-61Biological sex: AllType: InterventionalSponsor: Karolinska InstitutetUpdated: Jun 9, 2026Locations: 6
Eligibility criteria

Attended a Health dialogue visit to primary healthcare for patients 40-60 years... [+1]

diabetes [+4]

Status: Recruiting

Determining the Utility of a Behavioral Intervention in Chronic Migraine

This proposal will involve a pilot study to evaluate the feasibility, acceptability, and outcomes of a lifestyle behavior protocol in managing chronic migraine. Additionally, the proposal will investigate biomolecules that are uniquely involved in chronic migraine patients who respond to the protocol. Successful completion of this proposal will inform the design of a future full-scale behavioral clinical trial to control chronic migraine.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

have chronic migraine for a minimum of 1-year [+1]

other headache disorders including secondary headache disorders [+2]

Status: Recruiting

Reducing Blood Pressure in Mid-life Adult Binge Drinkers

This study has two phases: Phase 1 is to examine blood pressure, microvascular function, and sympathetic nerve activity in mid-life adult binge drinkers vs. alcohol abstainers/moderate drinkers. Phase 2 is to examine the effect of 8-week aerobic exercise training on blood pressure, microvascular function, and sympathetic nerve activity in mid-life adult binge drinkers

Participants needed: 55
Trial details
Age: 50-64Biological sex: AllType: InterventionalSponsor: The University of Texas at ArlingtonUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Men and women (50-64 years of age) who do not drink alcohol, who drink at modera... [+2]

a history of diabetes, cardiovascular disease, liver, or renal disease [+8]

Status: Recruiting

GENESIS Project: Generating Evidence on the Needs of Ecuadorian Adolescents

Background: Adolescence is a period of intensified emotional responses and occurs when mental health disorders commonly develop since adolescents are learning how to deal with powerful emotions. Globally, 15% of adolescents experience a mental disorder like depression or anxiety. However, adolescent mental health goes beyond mental disorders. It is state of mental well-being that allows individuals to deal with stressors, recognize their abilities, develop their activities well, and participate in society, providing a holistic approach that highlights the interplay between psychological well-being and other aspects of life. Given this perspective, a Lifestyle Medicine (LM) approach based on a multi-component framework is needed for assessing adolescents' mental health. This study aims to evaluate adolescents' (aged 14-19) mental health, identify and mitigate the risks of developing any mental health disorder as well as formulate comprehensive interventions to promote and increase their emotional wellbeing. Methods: Cross-sectional and longitudinal studies will be performed. Adolescents from Quito, Ecuador will be recruited using a simple random sampling technique. The minimum sample size is 385; however, to increase the precision of the estimates, a target sample of approximately 1000 participants will be established. Main outcome measure will be mental health using social determinants of health and lifestyle medicine factors. Conclusion: This research project will evaluate adolescents' mental health through a holistic and multiapproach evaluation and interrelate social determinants of health and lifestyle medicine variables to propose and design multidisciplinary strategies and interventions to prevent and mitigate mental health outcomes in adolescents. Additionally, the results will be useful in informing public health authorities to evaluate or modify current policies

Participants needed: 1,450
Trial details
Age: 14-19Biological sex: AllType: ObservationalSponsor: Universidad de Especialidades Espiritu SantoUpdated: Mar 20, 2026Locations: 1Duration: 5 Years
Eligibility criteria

be between 14 and 19 years old

have any disorder or treatment that contraindicated physical activity or that de... [+4]

Status: Recruiting

Nighttime Synchrony of Your Nutrition and Circadian Health

Sleep is an important factor for overall health. This study will see how different light exposure patterns and food intake impact a person's metabolism (how the body breaks down food) when sleeping is reduced. Participants will attend 6 to 8 in-person visits to the study clinic, including three overnight stays. People will complete surveys and medical tests. The study will last about 4 to 6 months.

Participants needed: 120
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Age: 18-35 years old; equal numbers of men and women [+2]

Clinically diagnosed sleep disorder or apnea hypopnea index (AHI) ≥5 [+14]

Status: Recruiting

Apple Health Study

The Apple Health Study aims to build a diverse and inclusive group of participants to help researchers advance our understanding of how signals and information collected from apps and devices relate to health and may be used to predict, detect, monitor, and manage changes in health. To enroll, US residents who have an iPhone can download the Apple Research app from the App Store and go through the introduction and informed consent for the Apple Health Study. This study is fully remote, and all are invited to enroll if the eligibility criteria are met. Participants will be asked to complete tasks and surveys, using their iPhone and Apple Research app which include: * Selecting the types of data they would like to share with the study such as health and sensor data * Completing tasks and surveys including areas such as personal demographic information, personal medical history, family history, and social determinants of health

Participants needed: 500,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Apple Inc.Updated: Jul 29, 2025Locations: 2Duration: 5 Years
Eligibility criteria

Be at least 18 years old (at least 19 years old in Alabama and Nebraska, at leas... [+5]

Share your iCloud account, iPhone, or devices that collect health data such as A...

Status: Recruiting

Lifestyle for the BRAin Health - Time Restricted Eating and Mindfulness

The study aims to evaluate the effects of a 9-month intervention combining yoga-based mindfulness techniques, cognitive training, and nutritional counseling on cognitive function, plasma markers of neurodegeneration (tau protein), physical fitness, and metabolism in older adults at increased risk of developing Alzheimer's disease.

Participants needed: 48
Trial details
Age: 60-80Biological sex: AllType: InterventionalSponsor: St. Anne's University Hospital Brno, Czech RepublicUpdated: Jun 27, 2025Locations: 1
Eligibility criteria

Age 60-80 years [+5]

Stroke or myocardial infarction within the past year [+9]

Status: Recruiting

TREC@TAMU Cancer Prevention Registry and Repository

This study collects health and genetic information to implement cancer prevention and treatment strategies.

Participants needed: 2,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Texas A&M UniversityUpdated: Feb 13, 2025Locations: 1Duration: 5 Years
Eligibility criteria

18 years of age and older, and, [+6]

Declines to participate or interact with staff/share their medical status. [+1]

Status: Recruiting

Effect of Sleep Extension on Ceramides in People with Overweight and Obesity

The overall goal is to determine how a sleep extension intervention (increasing time in bed) in individuals who maintain less than 6.5 hours sleep per night affects their plasma ceramides and insulin sensitivity. Participants will undergo a randomized controlled trial, with sleep extension (intervention) and healthy lifestyle (control) groups. The sleep extension is designed to increase participant's time in bed by 2 hours per night. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).

Participants needed: 70
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Dec 20, 2024Locations: 1
Eligibility criteria

Age: 18-45 years old; equal numbers of men and women [+2]

Clinically diagnosed sleep disorder or major psychiatric illness [+10]

Status: Recruiting

Circadian Intervention to Improve Cardiometabolic Health

The overall goal is to examine the efficacy of a circadian intervention in people with overweight and obesity and habitual short sleep duration (HSSD). Participants will undergo a randomized controlled trial, with circadian intervention and control (healthy lifestyle) groups. The circadian intervention is designed to reduce nighttime light exposure and after-dinner snack food intake. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).

Participants needed: 20
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Dec 20, 2024Locations: 1
Eligibility criteria

Age: 18-45 years old; equal numbers of men and women [+2]

Clinically diagnosed sleep disorder or major psychiatric illness [+9]

Status: Recruiting

Generation R Next - Optimaal Opgroeien

The aim of this randomized controlled trial is to improve birth outcomes and long-term outcomes in mother and child by optimizing lifestyle,nutrition and stress experience in the preconception period and early pregnancy in women and men The main research question that will be addressed is: Does an intervention focused on optimizing preconception and early pregnancy lifestyle, nutrition and stress improve the birth outcomes and long-term outcomes in mother and child? Participants will receive an individual lifestyle consultation at the start of the study. Depending on their study arm, participants will receive an additional lifestyle program focused on health during preconception and early pregnancy, coping with stress and adherence to a healthy(er) lifestyle. The given advices are based on national guidelines. Researchers will compare the intervention group and control group to see if (adherence to) this lifestyle program improve birth outcomes and long-term outcomes in mother and child.

Participants needed: 1,750
Trial details
Biological sex: FemaleType: InterventionalSponsor: Erasmus Medical CenterUpdated: Sep 4, 2024Locations: 1
Eligibility criteria

Planning a pregnancy or early pregnancy up to < 12 weeks [+3]

Temporary or complete withdrawal from participation [+1]

Status: Recruiting

Climbing Lifestyle Intervention for Modifying Physical Activity Behaviors: Pilot Study

The aim of this pilot study is to determine the effects of a 12-week indoor rock climbing training program on heart health, mental health, and behavioral health in generally healthy adults aged 18-35 years old who do not exercise. Participants will learn to rock climb using ropes on an indoor rock climbing wall and participate in the training program 2-3 days per week for 60 minutes each session over 12 weeks. Health outcomes will be measured at 4 time points over the course of the study (pre-intervention, 6-weeks/mid-intervention, 12-weeks/post-intervention, and 24-weeks post-intervention).

Participants needed: 12
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Northern Michigan UniversityUpdated: Jul 16, 2024Locations: 1
Eligibility criteria

Physically inactive [+4]

Physically active [+6]

Status: Recruiting

Using AI Text Messaging to Improve AHA's Life's Essential 8 Health Behaviors

The goal of our pragmatic clinical trial is to compare how well three different strategies might do to reduce risk factors for cardiovascular disease in patients experiencing health disparities. The three different strategies are: 1) text messages, 2) interactive chatbot messages, and 3) chatbot messages with proactive pharmacist support. To measure cardiovascular risk factors, the investigators are using the American Heart Association's Life's Essential 8 (LE8) factors-blood glucose, cholesterol, blood pressure, physical activity, body mass index, diet, and smoking. This study focuses on improving cardiovascular risk factors for individuals facing health disparities, such as ethnic minorities, limited English proficiency, and low-income groups. These groups are more likely to be seriously affected by cardiovascular diseases. Self-management, or an individual's roles in managing their own chronic disease, includes lifestyle changes, medication adherence. Improving patients' self-management has been shown to improve health behaviors, better disease control and improved patient outcomes. The main question this study aims to answer is if one of the strategies (texting, chatbot, or chatbot with pharmacist support) may improve patient self-management and patient outcomes. The investigators will enroll up to 2,100 patients from three health systems that serve large populations experiencing health disparities: Denver Health, Salud Family Health Centers, and STRIDE Community Health Center. The results might help researchers and health care systems find the best ways to involve patients with health disparities to managing their chronic cardiovascular disease.

Participants needed: 2,100
Trial details
Age: 18-89Biological sex: AllType: InterventionalSponsor: University of Colorado, DenverUpdated: Mar 22, 2024Locations: 3
Eligibility criteria

diagnosis of one or more of the following CV risk factors (i.e., hypertension, d... [+2]

patients who do not have cellphone; or [+3]