NCT07691112

Brief Summary

Chapman Reflex Points (CRPs) are small palpable nodules found within connective tissue that have traditionally been associated with dysfunction of internal organs and the autonomic nervous system. However, little is known about how commonly these findings occur in healthy individuals or whether they are associated with symptoms experienced by otherwise healthy people. The purpose of this study is to determine the prevalence of Chapman Reflex Points in young healthy adults and to evaluate whether the presence and distribution of these points are associated with self-reported visceral symptoms. Participants complete a standardized health questionnaire regarding recent and recurrent symptoms and undergo a blinded physical examination of established Chapman Reflex Point locations performed by a trained investigator. The results of this study may improve understanding of the physiological mechanisms underlying Chapman Reflex Points and help clarify their potential role in preventive osteopathic assessment and early identification of altered autonomic, lymphatic, fascial, or neuroendocrine function.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
101

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 4, 2020

Completed
6.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 26, 2026

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 27, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

June 30, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 8, 2026

Completed
Last Updated

July 8, 2026

Status Verified

June 1, 2026

Enrollment Period

6.3 years

First QC Date

June 30, 2026

Last Update Submit

July 6, 2026

Conditions

Keywords

Chapman Reflex PointsChapman ReflexesSomatic DysfunctionViscerosomatic ReflexesOsteopathic MedicineOsteopathic Manipulative MedicineFascial TissueMyofibroblastsLymphatic SystemLymphatic PhysiologyAutonomic Nervous SystemSympathetic Nervous SystemNeuroendocrine RegulationMechanotransductionConnective TissuePalpatory ExaminationVisceral SymptomsFasciaPreventive Medicine

Outcome Measures

Primary Outcomes (1)

  • Prevalence of Chapman Reflex Points

    The prevalence and distribution of Chapman Reflex Points identified during a standardized palpatory examination of established Chapman Reflex Point locations performed by a blinded trained investigator. The total number of Chapman Reflex Points observed per participant was recorded and summarized using descriptive statistics.

    through study completion, an average of 1 year

Secondary Outcomes (2)

  • Association Between Chapman Reflex Points and Visceral Symptom Clusters

    through study completion, an average of 1 year

  • Sex Differences in Chapman Reflex Point Prevalence

    through study completion, an average of 1 year

Other Outcomes (1)

  • Distribution of Organ System-Specific Chapman Reflex Points

    through study completion, an average of 1 year

Study Arms (1)

Healthy Young Adults

Participants were young adults who completed a standardized health questionnaire assessing demographic characteristics, medical history, lifestyle factors, and recent or recurrent visceral symptoms. Participants subsequently underwent a blinded palpatory examination of established Chapman Reflex Point locations performed by a trained investigator. No therapeutic intervention was administered. The study evaluated the prevalence and distribution of Chapman Reflex Points and their associations with self-reported visceral symptom clusters.

Procedure: Chapman Reflex Point Examination

Interventions

Participants underwent a standardized palpatory examination of established Chapman Reflex Point locations performed by a single trained investigator who was blinded to questionnaire responses. Consistent pressure application and examination duration were utilized to optimize reliability and reproducibility of palpatory findings. No therapeutic intervention, osteopathic manipulative treatment, medication administration, or other clinical intervention was provided as part of the study. Participants also completed a standardized health questionnaire assessing demographic characteristics, medical history, lifestyle factors, and recent or recurrent visceral symptoms.

Also known as: Chapman Reflex Point Assessment, Palpatory Examination of Chapman Reflex Points
Healthy Young Adults

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Young adult volunteers recruited from an osteopathic medical school community participated in this cross-sectional observational study. Participants completed a standardized questionnaire assessing demographic characteristics, medical history, lifestyle factors, and recent or recurrent visceral symptoms, followed by a blinded palpatory examination of established Chapman Reflex Point locations performed by a trained investigator. A total of 101 participants were enrolled, with a mean age of 27 years.

You may qualify if:

  • Adults aged 18 years or older.
  • Ability to understand the study procedures and provide informed consent.
  • Willingness to complete a standardized health questionnaire.
  • Willingness to undergo a blinded palpatory examination of established Chapman Reflex Point locations.

You may not qualify if:

  • Individuals younger than 18 years of age.
  • Inability or unwillingness to provide informed consent.
  • Inability or unwillingness to complete the health questionnaire.
  • Inability or unwillingness to undergo the palpatory examination.
  • Pregnancy.
  • Incomplete study data or questionnaire responses.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Touro College of Osteopathic Medicine - Harlem

New York, New York, 10027, United States

Location

MeSH Terms

Conditions

Autonomic Nervous System DiseasesLymphatic Diseases

Condition Hierarchy (Ancestors)

Nervous System DiseasesHemic and Lymphatic Diseases

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Osteopathic Manipulative Medicine

Study Record Dates

First Submitted

June 30, 2026

First Posted

July 8, 2026

Study Start

March 4, 2020

Primary Completion

June 26, 2026

Study Completion

June 27, 2026

Last Updated

July 8, 2026

Record last verified: 2026-06

Locations