Lubbock, TXNCT07189442Now EnrollingIRB Ready

Attention Deficit Hyperactivity Disorder (ADHD) Clinical Trial in Lubbock, TX

Access cutting-edge attention deficit hyperactivity disorder (adhd) treatment through this clinical trial at a research site in Lubbock. Study-provided care at no cost to qualified participants.

Sponsored by Texas Tech University Health Sciences Center

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Expert Care in Lubbock

Access attention deficit hyperactivity disorder (adhd) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related attention deficit hyperactivity disorder (adhd) treatment provided free

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Check if you qualify for this attention deficit hyperactivity disorder (adhd) clinical trial in Lubbock, TX

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Lubbock

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Lubbock site if eligible
  4. 4Begin participation

About This Attention Deficit Hyperactivity Disorder (ADHD) Study in Lubbock

This pilot study will test whether combining L-theanine and paraxanthine improves sustained attention, inhibitory control, and overall cognition in adults with ADHD and ASD. Two parallel randomized, single-blinded, repeated-measures crossover trials will be conducted. Participants will complete neuropsychological testing, fMRI scanning, and self-report measures following administration of the L-theanine-paraxanthine combination compared to placebo.

Sponsor: Texas Tech University Health Sciences Center

Who Can Participate

Inclusion Criteria

Adults (18+ years) diagnosed by a physician (per self-report) with ADHD or ASD \
Participants with a dual diagnosis and ASD and ADHD will be recruited but will only be included in the ASD group - their concurrent ADHD diagnosis will be included as an additional variable in exploratory analyses

Exclusion Criteria

Subjects with gross visual or auditory impairments that might limit their ability to perform neuropsychological tasks
Inability to read and follow written instructions
Physical, neurological, intellectual, or psychiatric impairments (except ADHD or ASD) that could affect cognitive and motor functions
Subjects on medications including antidepressants and antipsychotics that may affect performance in the tasks
Subjects on medications that are likely to interact with the administered substances, including regular intake of medication that could alter visual, auditory, cognitive, or motor functions (except stimulants)
History of head injury resulting in loss of consciousness/history of brain surgery
Subjects who have developed adverse effects when caffeine/paraxanthine /L-theanine/corn starch (will be in placebo) containing products were consumed
Subjects who are unwilling or unable to refrain from intake of L-theanine/ caffeine/ paraxanthine containing food or beverages within the 24 hours prior to each study visit
Intake of drugs containing caffeine, other phosphodiesterase inhibitors, or adenosine receptor blockers within the past 3 months
Intake of medications known to have pharmacological interactions with paraxanthine within the past 3 months
Current/past diagnosis of tics or other forms of dyskinesia
History of headache, drowsiness, anxiety, insomnia, or nausea following intake of caffeine or caffeine-containing beverages
Current/past history of smoking and/or alcohol or drug abuse
Subjects with absolute contraindications to undergo MRI after being screened by the TTNI safety screening sheet (Appendix)
Unwillingness or inability to entirely refrain from the use of electronic devices during study visits
Unwillingness or inability to follow written, on-screen, and verbal instructions given by the study team.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Lubbock?

Yes, this clinical trial (NCT07189442) has an active research site in Lubbock, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Attention Deficit Hyperactivity Disorder (ADHD) Treatment Options in Lubbock, TX

If you're searching for attention deficit hyperactivity disorder (adhd) treatment options in Lubbock, TX, this clinical trial (NCT07189442) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Lubbock research site is actively enrolling participants for this clinical trial. You'll receive care from experienced attention deficit hyperactivity disorder (adhd) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all attention deficit hyperactivity disorder (adhd) clinical trials near you to find additional studies recruiting in your area.

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