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NIH
Posted

PAR-25-207

Effectiveness Trials for Post-Acute Interventions and Services to Optimize Longer-term Outcomes (R01 Clinical Trial Required)

Summary

AI-generated

PAR-25-207: Effectiveness Trials for Post-Acute Mental Health Interventions

Research Focus

NIMH seeks effectiveness trials testing therapeutic and service delivery interventions for post-acute phase management of mental health conditions in youth, adults, and older adults. The post-acute phase encompasses continuation and maintenance treatment following acute episode management—consolidating treatment gains, managing residual symptoms, preventing relapse, and promoting long-term adherence and service engagement. Trials must be statistically powered to provide definitive effectiveness evidence and explicitly examine mechanisms of action, mediators, and predictors/moderators of intervention response. Research should address chronic or relapsing conditions (anxiety disorders, mood disorders, ADHD, psychotic disorders) where incomplete clinical response, symptom dissipation, and relapse risk remain significant challenges. Priority areas include pharmacological, psychosocial, and neuromodulation continuation/maintenance strategies; care transition facilitation; technology-assisted monitoring and adherence interventions; preventive approaches for gateway conditions; and population-level strategies using electronic health records (EHRs). Trials reducing disparities in post-acute outcomes for underserved populations (racial/ethnic minorities, rural residents, language/culturally isolated groups) are strongly encouraged.

At a Glance

  • Who can apply: Not stated (see NIH R01 eligibility guidelines)
  • Funding & project length: Not stated in overview
  • Award mechanism: R01 Research Project Grant (clinical trial required)
  • Key dates: Applications due February 5, 2025 (earliest); subsequent rounds June 5, 2025, October 5, 2025, and beyond through January 8, 2028
  • Best fit for: Clinical researchers in psychiatry, psychology, behavioral health, and health services studying post-acute mental health interventions; populations with chronic/relapsing mental illness; mixed-methods designs incorporating mechanism measurement

Key Facts

Deadline

Fri, January 7, 2028

Posted

Thu, October 31, 2024

Keywords

clinical trials
post-acute interventions
psychosocial interventions
pharmacological interventions
relapse prevention
treatment adherence
care transitions
health disparities
youth mental health
older adults
substance use disorders
psychotic disorders
technology-assisted interventions
mental health disorders
neuromodulation
maintenance therapy
mood disorders
anxiety disorders
ADHD
treatment mechanisms

Research Areas

MeSH
DiseasesC
Nervous System DiseasesC10Nutritional & Metabolic DiseasesC18Endocrine System DiseasesC19Immune System DiseasesC20Pathological Conditions & SymptomsC23
Chemicals & DrugsD
Hormones & AntagonistsD06Pharmaceutical PreparationsD26
Analytical/Diagnostic/Therapeutic TechniquesE
DiagnosisE01TherapeuticsE02
Psychiatry & PsychologyF
Behavior MechanismsF01Psychological PhenomenaF02Mental DisordersF03
Phenomena & ProcessesG
MetabolismG03Genetic PhenomenaG05
Anthropology/Education/SociologyI
Social SciencesI01
Health CareN
Health Care ServicesN02Health Care EconomicsN03Health Services AdministrationN04Health Care Quality & EvaluationN05
ANZSRC FoR
Biomedical & Clinical Sciences32
Clinical Sciences3202Neurosciences3209
Health Sciences42
Health Services & Systems4203Public Health4206
Human Society44
Policy & Administration4407
Psychology52
Applied & Developmental Psychology5201Clinical & Health Psychology5203

Gotchas (1)

Soft Block
planningprogram required components

Applicants must explicitly measure and test hypothesized change mechanisms/targets in the effectiveness trial context, not just measure outcomes. This is a required scientific component beyond standar

AI

93%

Source Text

Consistent with the NIMH experimental therapeutics approach, this NOFO is intended to support effectiveness trials that not only test the intervention effects on outcomes of interest but also explicitly inform understanding regarding whether the intervention engages associated change mechanisms that were previously identified under more controlled efficacy conditions, thereby reconfirming the intervention targets and testing whether previously identified change mechanisms are operative in the ef

AI-generated content — verify with the issuing agency’s official FOA/NOFO. Not endorsed by HHS.

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