Simpler Grants.gov #PAR-25-267

NIH NCCIH Multisite Feasibility Clinical Trials Grant for Mind and Body Interventions

This opportunity from the National Institutes of Health (NIH), via the National Center for Complementary and Integrative Health (NCCIH), supports multisite feasibility clinical trials of mind and body interventions. - Government Buyer: - National Institutes of Health (NIH) - National Center for Complementary and Integrative Health (NCCIH) - Products/Services Requested: - Investigator-initiated multisite feasibility clinical trials - Focus on mind and body interventions within complementary and integrative health - No specific OEMs or commercial vendors; this is a research grant - Unique/Notable Requirements: - Applicants must justify the need for multisite feasibility trials with preliminary data from prior single-site studies or published literature - Must address intervention fidelity, recruitment, adherence, protocol refinement, and data collection across multiple sites - Designed to generate data for planning full-scale clinical efficacy/effectiveness studies, pragmatic trials, or dissemination/implementation trials - Minimum award is $350,000; no cost sharing or matching required - Broad eligibility: educational, nonprofit, government, business, tribal, and minority-serving institutions - Place of Performance: - National Institutes of Health (NIH) - No product line items or OEMs are specified, as this is a grant for research services.

Description

This notice of funding opportunity invites applications for investigator-initiated clinical trials of complementary and integrative health approaches with physical and/or psychological therapeutic inputs in NCCIH-designated areas of high research priority. The proposed multisite feasibility clinical trial should provide new information necessary for planning and conducting a subsequent clinical efficacy or effectiveness study, pragmatic trial, or dissemination and implementation trial within NCCIH's mission. Applications must demonstrate the scientific necessity of the proposed research to design or plan a subsequent fully powered, full-scale clinical trial, addressing feasibility aspects such as intervention fidelity, recruitment, adherence, protocol refinement, and data collection across sites. The need for multisite feasibility trials should be justified by sufficient preliminary data from previous single-site feasibility or acceptability trials or published literature.

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