Clinical and Scientific Assessment of Pain and Painful Disorders
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02707029|
Recruitment Status : Recruiting
First Posted : March 14, 2016
Last Update Posted : September 16, 2019
Researchers want to better understand pain by studying people with and without different kinds of pain. To do this, researchers will expose people to pleasant and unpleasant sensations. They will ask them questions about their pain. Researchers also want to see if these people are eligible for other research studies at the National Center for Complementary and Integrative Health.
To study the experience of pain. Also to find people eligible to join other NIH studies.
People 12 years and older with and without pain disorders.
Participants will be screened by phone.
Participants will have one required visit. This may include:
- Medical history
- Physical exam
- Questionnaires about themselves and their pain experience
- Blood and urine tests
- MRI: They will lie on a table that slides into a cylinder. They will feel different sensations while completing tasks on a computer. This lasts 15 minutes to 2 hours.
Quantitative sensory testing: They will be exposed to different pictures, sounds, tastes, and smells. They will also be exposed to pleasant and unpleasant sensations. These could include:
- Burning, itching, or cold sensations
- Pressure and pinches
- Electrocardiogram: Stickers on the chest record heart activity.
- Straps placed around the chest to measure breathing.
- Small sensors on the fingers or palms to measure pulse and sweating.
Over the next 3 months, participants may have up to 4 other study visits. These last 2 to 4 hours each. They include repeats of some of the tests in the required visit.
Participants may be recorded at the visits.
|Condition or disease|
|Normal Physiology Pain|
The purpose of this study is to allow for the deep, broad, and targeted phenotyping of persons with or without pain disorders. This protocol will enable NCCIH investigators to describe the clinical aspects of pain disorders, collect scientific measurements for the purpose of making deep phenotypic descriptions, and use the collected data to perform descriptive analyses of pain disorders. The study will also facilitate obtaining information relevant to determining if a person is potentially eligible to participate in other research protocols at NIH, in particular those of the Laboratory of Clinical Investigation (LCI) at the National Center for Complementary and Integrative Health (NCCIH). The specific goals of this protocol are the following:
- To enable the clinical description and phenotyping of research volunteers, in particular those with pain disorders.
- To facilitate obtaining information relevant to determining potential eligibility of consenting volunteers to participate in other IRB-approved NIH protocols that focus on pain and related disorders.
- To perform descriptive analyses of painful experiences within discrete pain disorders.
The study population will consist of up to 10,000 persons with or without pain disorders, who seek to participate in research protocols at NIH, primarily those sponsored by NCCIH Division of Intramural Research investigators. Human beings of adolescence age or older (greater than or equal to 12 years) that are willing to provide assent and/or consent may participate in the study. This protocol is open to volunteers of any ethnicity, gender, or nationality.
The protocol is designed as a cross-sectional observational study. Participants will initially undergo an informed consent process and a core phenotyping evaluation, which includes a clinical evaluation from a Licensed Independent Practitioner (LIP) and questionnaires. Following the core evaluation, participants may undergo selected scientific measurements for phenotyping purposes. Phenotyping measurements can occur over the course of several months. On completion of the phenotyping measurements, participants will be discharged from the protocol. After completion, past participants may be contacted to undergo re-evaluation as appropriate.
The study will use a wide variety of measurement tools for phenotyping purposes. These include: vital signs, medical history, physical exam, medical record review, qualitative pain interview, patient reported outcome measurements, psychophysical and behavioral measurements, clinical laboratory measurements, structural and functional imaging assessments using magnetic resonance imaging, and psychophysical measurements.
In summary, the NCCIH phenotyping protocol will enable investigators to obtain detailed clinical descriptions and collect phenotyping measurements from research volunteers, in particular those with pain disorders. It will collect information on research volunteers that, with consent, can be used to determine potential eligibility in other IRB-approved protocols. The study will allow NCCIH investigators to perform descriptive research on pain disorders for use in hypothesis generation.
|Study Type :||Observational|
|Estimated Enrollment :||10000 participants|
|Official Title:||Clinical and Scientific Assessment of Pain and Painful Disorders|
|Actual Study Start Date :||July 22, 2016|
|Estimated Primary Completion Date :||February 9, 2026|
|Estimated Study Completion Date :||February 9, 2026|
Persons, with or without pain disorders
Adults and adolescents with or without pain disorders.
- To enable for the deep, broad, and targeted phenotyping of individuals, in particular those with rare and unusual pain disorders. [ Time Frame: 36 months ]Data are to be collected via medical history, physical examinations, questionnaires, laboratory samples and MRI imaging.
- To facilitate obtaining information relevant to determining potential eligibility in IRB-approved NIH protocols, in particular those of the Clinical Investigations Branch of NCCIH. [ Time Frame: 36 months ]Data are to be collected via medical history, physical examinations, questionnaires, laboratory samples and MRI imaging.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02707029
|Contact: Adebisi O Ayodele, C.R.N.P.||(301) firstname.lastname@example.org|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) 800-411-1222 ext TTY8664111010 email@example.com|
|Principal Investigator:||Mary C Bushnell, Ph.D.||National Center for Complementary and Integrative Health (NCCIH)|