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Understanding Stress and Alcohol Use in College-Aged Women
Official Title Examining the Role of Sensitivity to Uncertain Threat and Alcohol Response in Risk for AUD following Sexual Assault in College WomenPurpose
The purpose of this study is to better understand how stress relates to alcohol use in biological females aged 21-29.
Participation in the study includes three in-person visits and the completion of daily phone surveys across 21 days while wearing a biosensor, which is similar to a Fitbit or smart watch. The first lab visit includes screening and orientation with blood draw, EKG, and sensory tasks. The second and third lab visits include sensory tasks and intravenous alcohol or placebo (a saline solution) administration. Participation in the study occurs over a period of 7 weeks.
Could this study be right for you?
Inclusion Criteria:
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Biological female
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21-29 years old
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At least a high school education
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Fluency in English
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Drink alcohol regularly
(partial list of inclusion criteria)
Exclusion Criteria:
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Current pregnancy
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Lifetime history of psychosis
(partial list of exclusion criteria)
Age Range
21 - 29 years -
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Study of Pain Sensitivity and Responses to Alcohol
Official Title Pain Sensitivity, Alcohol-Induced Analgesia, and Heavy Drinking in Individuals with Opioid Use DisorderPurpose
The purpose of this study is to better understand how pain and related emotions change during sobriety and after drinking alcohol.
The length of the study is approximately 4 weeks and will include three on-campus lab visits at Ohio State's Medical Campus. The first lab visit includes screening and orientation with blood draw, EKG, and sensory tasks. The second and third lab visits include sensory tasks and intravenous alcohol or placebo (a saline solution) administration. The total time commitment of the study is approximately 17 hours.
Could this study be right for you?
Inclusion Criteria:
For this study, we are looking for people ages 21–65 who meet one of the following:
- Drink alcohol regularly
- Drink alcohol regularly and use opioids
- Occasionally drink alcohol and use opioids
(partial list of inclusion criteria)
Exclusion Criteria:
- Sensitivity to alcohol
- Current pregnancy
- Current or past diagnosis of mania or psychosis
(partial list of exclusion criteria)
Age Range
21 - 65 years -
Online Caregiver Focus Group Study
Official Title Development of Internet-Based Mind-Body Trainings for Spousal Caregivers of Persons Living with Dementia (Caregiver iMBT)Purpose
The main goal of this study is to better understand the experiences of caregivers. We are interested in the mental and physical health of spousal caregivers of persons living with dementia. We will learn about caregiver experiences using online focus groups, which are discussions where a group of people get together to talk about a particular topic. The information we learn from the focus groups will be used to adapt existing internet-based mind-body interventions to promote caregiver wellbeing.
Study participation will typically take place over 3 to 4 months. The total time commitment will be up to 6 hours, involving a brief eligibility screening, two 2-hour focus group sessions, and online questionnaires lasting up to 1 hour.
Could this study be right for you?
- You provide weekly care for your spouse who has a formal diagnosis of dementia
- You do not have any of the following: Alzheimer's disease, vascular dementia, Parkinson's disease, Lewy body disease, fronto-temporal lobar degeneration
- You are a fluent English speaker
- You have access to the internet and an at-home computer with a working microphone and video camera
- You have adequate hearing for focus group participation
- You live in the state of Ohio
Age Range
50 years and up -
Understanding the Link Between Chronic Pain and Suicide Risk
Official Title Modifiable Mechanisms Linking Chronic Pain to Suicide RiskPurpose
The purpose of this study is to better understand how certain thoughts, feelings, and responses to pain may be related to thoughts of suicide in people with chronic pain.
Participants will complete an online screening session that will involve a short interview and questionnaires which will take approximately 3.5 hours and a 2.5-hour in-person lab visit that will include EMG and EEG and a pain pressure test. After, participants will be asked to complete daily app-based questionnaires on their phone for 21 days.
Could this study be right for you?
- Currently experiencing chronic pain
- Have recently felt that life is not worth living or that you would be better off dead
Age Range
18 - 65 years -
The OSU Sleep Study - An Online Parent Training Research Study for Insomnia/Sleep Problems in Young Children with Autism Spectrum Disorder
Official Title A Parent-Mediated Telehealth Intervention for Insomnia in Young Autistic ChildrenPurpose
Insomnia is a common problem for young children with autism spectrum disorder (ASD) and their families. The purpose of this study is to compare the benefits of sleep parent training (SPT) program to a structured parent education program (SPE) for insomnia improvement in young children with autism spectrum disorder.
Could this study be right for you?
You may be eligible if your child:
1. Has a diagnosis of Autism Spectrum Disorder
2. Has significant Sleep Disturbance
3. Is free of a significant health problem
4. Is on stable medication
Age Range
3 - 7 years -
Emotional Regulation among Distressed Young Adults
Official Title Emotion Regulation Training to Reduce Cardiovascular Disease Risk Among Distressed Young Adults: A Single-Session DesignPurpose
This study looks at how learning to manage emotions can improve your mental and physical health.
You will meet with a research team member for an interview about your mental health. If you qualify, we will take a few drops of blood from a finger prick and check your heart rate and blood pressure. You will also learn some emotional regulation skills for handling tough emotions and fill out surveys about yourself. For two weeks after, you'll answer short surveys on your phone five times a day. Then you'll come back for one more short visit.
Could this study be right for you?
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Have a depressive or anxiety disorder
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Are not currently receiving mental health counseling
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Read and understand English
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Are willing to have a finger prick for a blood sample
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Free from immune-related or heart-related diseases
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Own or have access to a smartphone
Age Range
18 - 39 years -
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Anxiety and Inflammation in Adults
Official Title Inflammation in adults with anxiety disordersPurpose
This study looks at how anxiety can affect your immune health.
You will meet with a research team member for an interview about your mental health. If you qualify, we will take a few drops of blood from a finger prick. Then you will fill out some surveys about yourself and your mental health.
Study visits will last approximately 2 hours. Once the 2-hour visit is complete, you will be released from the study. There will be no long-term follow-up after completion of research related procedures.
Could this study be right for you?
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Have an anxiety disorder (social anxiety disorder, specific phobia, panic disorder, agoraphobia, generalized anxiety disorder).
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Are 18 years or older
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Read and understand English
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Free from immune-related diseases
Age Range
18 years and up -
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Effectiveness of Pairing a Keto Diet with Psychotherapy for PTSD
Official Title Enhancing PTSD Recovery with Metabolic-Augmented PsychotherapyPurpose
To test whether a personalized ketogenic program in combination with cognitive processing therapy (CPT) can improve symptoms of post-traumatic stress disorder (PTSD).
The study will involve 11 weeks of a personalized ketogenic program guided by a dietician, 10 sessions of CPT, interviews, questionnaires, and wearing sensors to track your stress, sleep, glucose, and ketones.
Could this study be right for you?
- 18 years or older
- Able to attend in-person visits to OSU once per week for 12 weeks
- Meet diagnostic criteria for PTSD (prior diagnosis is NOT required, all individuals will be evaluated by the study team)
Age Range
18 years and up -
Single-Dose Investigational Drug Study for Depression and Anxiety
Official Title A Randomized, Double-Blind, Placebo-Controlled Mechanistic Study to Assess a Single Oral Dose of CYB003 in Participants with Major Depressive Disorder (MDD) and Moderate to Severe AnxietyPurpose
The aim of this study is to determine the effects of one administration of the psychedelic compound CYB003 on depression and anxiety symptoms as well as its effects on brain function.
Could this study be right for you?
1. Currently have depression with moderate to severe anxiety
2. Are currently taking an antidepressant and your symptoms have not improved enough
3. Have been on the same antidepressant dose for about 1 month
Age Range
21 - 65 years -
A Study about how virtual Yoga sessions affect symptoms and quality of life in patients with diabetic gastroparesis
Official Title The Effect of Virtual Yoga Intervention on Symptom Severity and Quality of Life in Patients with Diabetic GastroparesisPurpose
The purpose of this research study is to understand how virtual Yoga sessions conducted 4 days a week for 12 weeks affect digestive symptoms and quality of life in those suffering from gastroparesis due to diabetes mellitus.
Could this study be right for you?
- Able to understand English
- Must have been diagnosed with gastroparesis
- Must have type 1 or type 2 diabetes mellitusAge Range
18 - 65 years