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Trial Phase
Trial Status
Paid Participation
43 Adhd Trials near West Virginia
Power is an online platform that helps thousands of Adhd patients discover FDA-reviewed trials every day. Every trial we feature meets safety and ethical standards, giving patients an easy way to discover promising new treatments in the research stage.
Learn More About PowerCentanafadine for ADHD
Trial Details
Key Eligibility Criteria
680 Participants Needed
SPN-812 for ADHD
Trial Details
Key Eligibility Criteria
286 Participants Needed
MomMA Intervention for ADHD
Trial Details
Key Eligibility Criteria
120 Participants Needed
Transcranial Focused Ultrasound for Impulsivity
Trial Details
Key Eligibility Criteria
31 Participants Needed
MomMA Intervention for ADHD
Trial Details
Key Eligibility Criteria
10 Participants Needed
Interaction Training for Childhood Behavior
Trial Details
Key Eligibility Criteria
264 Participants Needed
Sensory Intervention for Sleep Issues in ADHD
Trial Details
Key Eligibility Criteria
30 Participants Needed
Quillivant XR for ADHD in Down Syndrome
Trial Details
Key Eligibility Criteria
100 Participants Needed
Digital Therapy Apps for Childhood Behavior Problems
Trial Details
Key Eligibility Criteria
324 Participants Needed
Stimulant Medications for ADHD in Autism Spectrum Disorder
Trial Details
Key Eligibility Criteria
500 Participants Needed
Implementation Support Strategies for Disruptive Behaviors
Trial Details
Key Eligibility Criteria
450 Participants Needed
Sleep-Focused Parenting Intervention for Preschoolers with ADHD
Trial Details
Key Eligibility Criteria
50 Participants Needed
Emotional Regulation Intervention for Adolescents
Trial Details
Key Eligibility Criteria
60 Participants Needed
Implementation Strategy for HIV Prevention in Drug Addiction
Trial Details
Key Eligibility Criteria
536 Participants Needed
Extended-release vs Sublingual Buprenorphine for Opioid Use Disorder
Trial Details
Key Eligibility Criteria
144 Participants Needed
PrEP Adherence Strategies for HIV Prevention in Women
Trial Details
Key Eligibility Criteria
125 Participants Needed
rTMS for Opioid Use Disorder
Trial Details
Key Eligibility Criteria
20 Participants Needed
Buprenorphine for Opioid Addiction during Pregnancy
Trial Details
Key Eligibility Criteria
140 Participants Needed
LIFU for Cocaine Use Disorder
Trial Details
Key Eligibility Criteria
30 Participants Needed
Naltrexone + Bupropion for Methamphetamine Addiction
Trial Details
Key Eligibility Criteria
360 Participants Needed
Why Other Patients Applied
"I have dealt with voice and vocal fold issues related to paralysis for over 12 years. This problem has negatively impacted virtually every facet of my life. I am an otherwise healthy 48 year old married father of 3 living. My youngest daughter is 12 and has never heard my real voice. I am now having breathing issues related to the paralysis as well as trouble swallowing some liquids. In my research I have seen some recent trials focused on helping people like me."
"I changed my diet in 2020 and I’ve lost 95 pounds from my highest weight (283). I am 5’3”, female, and now 188. I still have a 33 BMI. I've been doing research on alternative approaches to continue my progress, which brought me here to consider clinical trials."
"I've been struggling with ADHD and anxiety since I was 9 years old. I'm currently 30. I really don't like how numb the medications make me feel. And especially now, that I've lost my grandma and my aunt 8 days apart, my anxiety has been even worse. So I'm trying to find something new."
"I've tried several different SSRIs over the past 23 years with no luck. Some of these new treatments seem interesting... haven't tried anything like them before. I really hope that one could work."
"My orthopedist recommended a half replacement of my right knee. I have had both hips replaced. Currently have arthritis in knee, shoulder, and thumb. I want to avoid surgery, and I'm open-minded about trying a trial before using surgery as a last resort."
Sparrow Link Device for Opioid Withdrawal Syndrome
Trial Details
Key Eligibility Criteria
50 Participants Needed
Combined Adductoplasty™ and Lapiplasty® Surgery for Bunions
Trial Details
Key Eligibility Criteria
80 Participants Needed
Extended Release Buprenorphine for Opioid Use Disorder
Trial Details
Key Eligibility Criteria
344 Participants Needed
Tirzepatide for Opioid Use Disorder
Trial Details
Key Eligibility Criteria
310 Participants Needed
EHR Nudges for Opioid Overdose
Trial Details
Key Eligibility Criteria
1350 Participants Needed
Couples Motivational Interviewing for Substance Abuse and HIV Risk
Trial Details
Key Eligibility Criteria
360 Participants Needed
Pain Self-Management for Opioid Use Disorder
Trial Details
Key Eligibility Criteria
204 Participants Needed
Buprenorphine for Opioid Addiction during Pregnancy
Trial Details
Key Eligibility Criteria
97 Participants Needed
Buprenorphine for Opioid Use Disorder in Pregnancy
Trial Details
Key Eligibility Criteria
200 Participants Needed
Lacosamide for Chronic Pancreatitis
Trial Details
Key Eligibility Criteria
24 Participants Needed
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Frequently Asked Questions
How much do Adhd clinical trials in West Virginia pay?
Each trial will compensate patients a different amount, but $50-100 for each visit is a fairly common range for Phase 2–4 trials (Phase 1 trials often pay substantially more). Further, most trials will cover the costs of a travel to-and-from the clinic.
How do Adhd clinical trials in West Virginia work?
After a researcher reviews your profile, they may choose to invite you in to a screening appointment, where they'll determine if you meet 100% of the eligibility requirements. If you do, you'll be sorted into one of the treatment groups, and receive your study drug. For some trials, there is a chance you'll receive a placebo. Across Adhd trials in West Virginia 30% of clinical trials have a placebo. Typically, you'll be required to check-in with the clinic every month or so. The average trial length in West Virginia for Adhd is 12 months.
How do I participate in a study as a "healthy volunteer"?
Not all studies recruit healthy volunteers: usually, Phase 1 studies do. Participating as a healthy volunteer means you will go to a research facility in West Virginia several times over a few days or weeks to receive a dose of either the test treatment or a "placebo," which is a harmless substance that helps researchers compare results. You will have routine tests during these visits, and you'll be compensated for your time and travel, with the number of appointments and details varying by study.
What does the "phase" of a clinical trial mean?
The phase of a trial reveals what stage the drug is in to get approval for a specific condition. Phase 1 trials are the trials to collect safety data in humans. Phase 2 trials are those where the drug has some data showing safety in humans, but where further human data is needed on drug effectiveness. Phase 3 trials are in the final step before approval. The drug already has data showing both safety and effectiveness. As a general rule, Phase 3 trials are more promising than Phase 2, and Phase 2 trials are more promising than phase 1.
Do I need to be insured to participate in a Adhd medical study in West Virginia?
Clinical trials are almost always free to participants, and so do not require insurance. The only exception here are trials focused on cancer, because only a small part of the typical treatment plan is actually experimental. For these cancer trials, participants typically need insurance to cover all the non-experimental components.
What are the newest Adhd clinical trials in West Virginia?
Most recently, we added MomMA Intervention for ADHD, Interaction Training for Childhood Behavior and Tirzepatide for Opioid Use Disorder to the Power online platform.
How to manage ADHD without Adderall?
Think of ADHD care without Adderall as three pillars: 1) proven skills training such as cognitive-behavioral therapy or parent/teacher coaching, which meta-analyses show can meaningfully cut inattentive and impulsive symptoms; 2) daily habits that boost brain chemicals—consistent aerobic exercise, 7-9 hours of sleep, and a balanced, low-sugar diet—each backed by research to modestly improve focus; 3) targeted add-ons (omega-3 fish-oil supplements, mindfulness practice, or professionally guided neurofeedback) that have small but credible benefits for some people. Work with a clinician to combine, test, and adjust these pieces every few months so you know what is actually helping and can add non-stimulant medicines later if needed.
Are we over diagnosing ADHD?
Rates of ADHD diagnosis have climbed, and studies confirm that some children—especially the youngest in a class or from more advantaged families—get the label and medication they may not truly need. At the same time, girls, adults, and many minorities with real symptoms are often missed, so the issue is less “too much” diagnosis overall and more “diagnosis in the wrong people.” Asking for a full evaluation that checks symptoms in several settings and rules out sleep, mood, or learning problems is the best safeguard against both mistakes.
What is the latest research on ADHD?
Recent work is mapping ADHD on two fronts: cause and treatment. On the biology side, a 2023 genome-wide study involving >40 000 people pinpointed 30+ gene regions, MRI scans show disrupted communication between attention- and reward-circuits, and several studies find distinct gut-bacteria patterns in both kids and adults—together suggesting ADHD arises from a mix of genes, brain-network wiring and (still-early) gut influences. Translating this, clinicians now have newer options beyond classic stimulants—FDA-approved viloxazine XR, long-acting patches, the prescription video-game EndeavorRx, and small but promising trials of neurofeedback and cognitive training—so ask your doctor about standard medications plus these emerging tools that may soon allow more personalized care.
Does Johnny Depp have ADHD?
There is no credible public record—interview, court document, or medical statement—showing that Johnny Depp has been formally diagnosed with ADHD; the claim stems from unsourced online lists that repeat each other. Until Depp or a qualified clinician confirms otherwise, any statement that he “has ADHD” should be treated as unverified speculation; if you need information about ADHD, rely on a licensed health professional, not celebrity rumors.
What is the 80 20 rule ADHD?
For someone with ADHD, the 80/20 rule means spotting the 20 % of tasks or habits that create about 80 % of your desired results—then protecting time and attention to do those first, ideally when your medication or energy is at its peak. This cuts overwhelm because you give yourself permission to ignore low-impact busywork and instead break the high-impact tasks into small, doable steps (using timers, alerts, or an accountability partner). Think of it as a focusing lens, not a cure; pair it with your regular ADHD treatments and adjust the “vital 20 %” as your goals change.
Is ADHD a disability?
Yes—ADHD is treated as a disability when the symptoms are strong enough to “substantially limit” everyday activities like focusing, learning, or working, which is exactly how U.S. laws such as the ADA, Section 504, and Social Security define disability. A diagnosis alone isn’t enough; you need documentation that the condition is causing real-world problems, after which schools, employers, or benefit programs must consider reasonable supports (extra time, quiet workspace, flexible scheduling, etc.). If you think ADHD is holding you back, gather medical records and examples of how it affects your tasks and formally ask for accommodations or benefits under the relevant program.
What makes ADHD people happy?
Studies show that people with ADHD feel happiest when four things line up: (1) their core symptoms are tamed with medication and/or ADHD-specific therapy, (2) predictable routines, reminders, exercise, and good sleep cut daily chaos, (3) they spend real time in activities that match their high interests and creativity, and (4) they’re surrounded by family, friends, or support groups that understand ADHD rather than shame it. Put simply: treat the symptoms, externalize organization, lean into your passions, and stay connected to people who “get” you—those combined levers consistently raise quality-of-life scores for both kids and adults with ADHD.
How much weight did you lose on ADHD medication?
Weight loss on stimulant ADHD medicines is usually modest and highly individual—clinical trials show average drops of about 3–5 lb (1–2 kg) in the first month and roughly 6–10 lb (3–4 kg) over the first 3–6 months, with only one-third of people losing more than 5 % of their starting weight before the effect levels off. Weigh yourself (or your child) weekly; if you see more than a 10 % fall from baseline or a slowdown in growth, talk with the prescriber about dose timing, nutrition strategies, or switching to a non-stimulant option.
What makes ADHD worse in adults?
Anything that further strains the brain’s self-regulation system can flare adult ADHD: lack of sleep or exercise, chronic stress, unmanaged anxiety/depression, inconsistent medication or substance use, hormonal shifts, and chaotic, screen-heavy environments. Focus on the controllables—protect 7-9 h of sleep, move daily, eat regular balanced meals, keep spaces and schedules simple, treat co-existing mood issues, and take medication exactly as prescribed—then review persisting problems with your clinician.
Is there still ADHD med shortage?
Yes—into 2024 many pharmacies still report spot shortages of popular stimulant ADHD medicines, especially immediate-release Adderall, several methylphenidate/Concerta generics, and some Vyvanse doses, because factory slow-downs and federally capped production haven’t kept up with rising prescriptions. Availability varies week-to-week and by location, so call a few pharmacies early, ask if a different strength or brand is in stock, and have your prescriber ready to adjust the prescription or discuss a short-term non-stimulant alternative if needed.