Opportunity
Simpler Grants.gov #PAR-24-275
NIH Solicitation for Clinical Coordinating Center for Multi-Site Mind and Body Clinical Trials
Buyer
National Institutes of Health
Posted
September 11, 2024
Respond By
July 14, 2026
Identifier
PAR-24-275
NAICS
541715
The National Institutes of Health (NIH), part of the U.S. Department of Health and Human Services, is seeking a Clinical Coordinating Center (CCC) to lead multi-site clinical trials on mind and body interventions in priority research areas for the National Center for Complementary and Integrative Health (NCCIH). - Government Buyer: - National Institutes of Health (NIH), Department of Health and Human Services - National Center for Complementary and Integrative Health (NCCIH) - Products/Services Requested: - Clinical Coordinating Center (CCC) to develop and implement fully powered Phase III or later multi-site clinical trials - Includes project management, participant recruitment and retention, performance milestones, scientific conduct, and dissemination of results - Data Coordinating Center (DCC) application required, providing a data analysis and management plan - Unique/Notable Requirements: - Applicants must submit both CCC and DCC applications for consideration - Focus on mind and body interventions (physical, psychological, nutritional) in NCCIH priority areas - Emphasis on comprehensive scientific and operational planning - Open to research centers and institutions; no specific OEMs or commercial vendors required - No OEMs or commercial product vendors are specified, as this is a cooperative agreement grant for research institutions.
Description
This notice of funding opportunity encourages applications for investigator-initiated multi-site clinical trials to study the effects of complementary and integrative health approaches with physical and/or psychological therapeutic inputs, and/or multicomponent interventions including physical, psychological, and/or nutritional approaches in NCCIH-designated priority areas. Clinical Coordinating Centers (CCC) are expected to develop and implement fully powered multi-site clinical trials (Phase III and beyond) with comprehensive scientific and operational plans. Applications must describe project management, participant recruitment and retention strategies, performance milestones, scientific conduct, and dissemination of results. A Data Coordinating Center (DCC) application is required to be submitted simultaneously for consideration.