NIH-funded research R01 grant

Nonstimulant-First vs Stimulant-First ADHD Treatment in Adults

Official title: Randomized controlled trial comparing nonstimulant-first vs stimulant-first strategies in treating ADHD in adults

Funded at Upstate Medical University · NIH-11457732 · Data updated 2026-11-12

This trial tests whether starting ADHD treatment with a nonstimulant medication works as well as starting with a stimulant for adults with ADHD.

More Randomized Controlled Trial research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUpstate Medical University
NIH-funded
Lab location1 site (Syracuse, United States)
Project startSeptember 10, 2026
Project endAugust 31, 2031
Funding year2026
Award (this year)$839,468
NIH project number1R01MH146143-01
Project IDNIH-11457732 on NIH RePORTER

Who could benefit from this research

Could help

Adults diagnosed with ADHD who are considered candidates for pharmacologic treatment.

Less likely to help

Adults with ADHD who are clearly nonresponsive to nonstimulants or stimulants, or those with contraindications to these medications, may receive limited benefit.

What this research studies

Adult patients with ADHD will be randomized to start either a nonstimulant or a stimulant medication and will be followed for 12 weeks to compare effectiveness and acceptability of the two approaches in real-world clinical settings. The study uses a pragmatic design to reflect typical care, measuring response to treatment and patient satisfaction. Researchers will also explore whether coexisting anxiety or depression changes which approach works best. The findings could help guide physicians and patients in choosing the first-line medication strategy.

Why it matters

Potential benefit: If successful, the nonstimulant-first approach could offer another viable option for adults with ADHD, potentially improving outcomes and reducing concerns about stimulant use.

How similar studies have gone: Previous real-world trials suggest that different first-line strategies can be feasible, but results for adults with ADHD are still being clarified.

Where this research is happening

  • Upstate Medical University
    Syracuse, United States
    Active

Researchers

  • Principal investigator: Faraone, Stephen V — Upstate Medical University
  • Study coordinator: Faraone, Stephen V

Related research

Other NIH-funded projects on the same topics.

  • Cognitive behavioral therapy and trazodone for insomnia phenotypes with high blood pressure

    A clinical study tests how CBT-I and the sleep drug trazodone work for adults with insomnia and high blood pressure, focusing on a specific sleep duration pattern.

    NIH research Pennsylvania State Univ Hershey Med Ctr · Hershey, United States · NIH-11635771

  • Shorter antifungal treatment for kids with candidemia

    A multi-center pediatric trial tests whether a shorter, 7 extra days of antifungal therapy after an initial 7 days is just as good as the standard 14-day approach for kids with candidemia who are improving on echinocandin therapy.

    NIH research Arkansas Children's Hospital Res Inst · Little Rock, United States · NIH-11606539

  • Short Course vs Standard Course Antifungal Therapy for Pediatric Candidemia

    This study tests whether a shorter 7-day total antifungal treatment after an initial 7 days of echinocandin therapy is as effective as the usual 14-day course for children with candidemia.

    NIH research Arkansas Children's Hospital Res Inst · Little Rock, United States · NIH-11606535

  • Shorter antifungal treatment for kids with candidemia

    A multi-center study tests whether kids with candidemia can finish treatment earlier after an initial week of antifungal therapy than the standard two weeks total.

    NIH research Arkansas Children's Hospital Res Inst · Little Rock, United States · NIH-11606531

  • Shorter antifungal treatment for kids with candidemia

    This study tests whether children with candidemia can finish treatment after 7 days of an echinocandin if they are improving, instead of completing a full 14 days.

    NIH research Arkansas Children's Hospital Res Inst · Little Rock, United States · NIH-11606505

  • Shorter antifungal course for kids with candidemia

    A multi-center study tests whether 7 extra days of antifungal therapy after an initial week of treatment can be shortened safely for children with candidemia.

    NIH research Arkansas Children's Hospital Res Inst · Little Rock, United States · NIH-11606502

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.