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Algometer and Category II Pelvic Blocking and Cranial Protocol

L

Logan College of Chiropractic

Status

Completed

Conditions

Sacroiliac Joint Dysfunction
Pain

Treatments

Procedure: Category II Pelvic Blocking and Cranial
Procedure: Cranial Only
Procedure: Category II Pelvic Blocking

Study type

Interventional

Funder types

Other

Identifiers

NCT00649753
SR0225080125

Details and patient eligibility

About

The purpose of this study is to evaluate the relationship of pelvic blocking and protocol for cranial adjusting with specific pain areas as outlined by Dr. Bertrand DeJarnette in the Category II/sacroiliac protocol. An algometer will be used to determine the level of pain at specific points before and after each treatment of pelvic blocking with or without cranial adjusting.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Logan student, staff or faculty
  • Age 18 - 60
  • No chiropractic adjustment 2 weeks prior to beginning the study
  • Show the DeJarnette Category II indicators

Exclusion criteria

  • Previous lower extremity, first rib and spine injury, surgery
  • Local infection, injury or other malignancy affecting the lower extremity and the nervous system
  • Unstable joints of the lower extremity and/or first rib and/or spine
  • Prescription or herbal muscle stimulants, relaxants, etc. that could affect the nervous system
  • Contraindication to DeJarnette Category II Pelvis Blocking
  • Pregnancy
  • Significant lower lumbar involvement
  • Diabetes, shortness of breath on light physical activity, cardiovascular disease
  • Numbness and/or tingling in the lower extremities

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 4 patient groups

A
No Intervention group
B
Experimental group
Treatment:
Procedure: Category II Pelvic Blocking
C
Experimental group
Treatment:
Procedure: Category II Pelvic Blocking and Cranial
D
Experimental group
Treatment:
Procedure: Cranial Only

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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