Screening Protocol

Part of paid clinical trials in Bethesda, Maryland.

Sponsor
National Center for Complementary and Integrative Health (NCCIH)
Study ID
NCT07712874
Status
Not Yet Recruiting

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Conditions

  • Pain

Eligibility Criteria

Sex
ALL
Age
12 Years - 100 Years
Healthy Volunteers
Accepted

Study Details

This study is a screening evaluation for volunteers who are interested in participating in National Center for Complementary and Integrative Health (NCCIH) research studies about pain and related processes, such as emotion, mood, and decision-making. Screening may include review of medical history, physical exam, vital signs, questionnaires, blood and urine tests, and optional sensory testing to better understand pain and related symptoms. The purpose is to identify and characterize healthy volunteers and people with pain who may be eligible for future NCCIH research studies. This screening study does not test a treatment and has no formal hypothesis.

Key Dates

First listed
Jul 20, 2026
Start date
Aug 1, 2026
Status verified
Jul 2026
Primary completion
Jul 2, 2050
Completion
Jul 2, 2050

Study Design

Enrollment
10,000 participants (estimated)

Arms

  • Arm: Healthy Volunteers
    Individuals screened under this protocol who are determined to be in good health and without a pain history that would classify them as a participant with pain. These participants may be considered for future NCCIH studies as healthy controls.
  • Arm: Participants With Pain
    Individuals screened under this protocol who have a current or prior pain history or pain symptoms identified through medical history, examination, questionnaires, or sensory testing. These participants may be considered for future NCCIH studies of pain and related processes.

Primary Outcome Measure

Screening classification of participant health and pain status [ Time Frame: Up to 3 days ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
National Institutes of Health Clinical CenterBethesdaMaryland20892
NIH Clinical Center Office of Patient Recruitment (OPR)
800-411-1222

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