NCT00741000

Brief Summary

Observe the effects of Cervical Stairstep on Cervical Spine Range of Motion

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P50-P75 for phase_1

Timeline
Completed

Started Jul 2008

Shorter than P25 for phase_1

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2008

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 21, 2008

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 25, 2008

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2008

Completed
Last Updated

August 25, 2008

Status Verified

August 1, 2008

Enrollment Period

3 months

First QC Date

August 21, 2008

Last Update Submit

August 22, 2008

Conditions

Range of Motion, Articular

Outcome Measures

Primary Outcomes (1)

  • Cervical Range of Motion

    Pre and post treatment

Secondary Outcomes (1)

  • Neck Disability Index

    pre and post treatment

Study Arms (1)

Experimental

EXPERIMENTAL

Cervical low force mobilization procedure.

Procedure: Cervical Stairstep

Interventions

Cervical StairstepPROCEDURE

Cervical low force mobilization procedure.

Experimental

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • students and faculty between ages 18 and 50

You may not qualify if:

  • current neck pain (as measured by the Neck Disability Index (NDI) and utilizing Jackson's and maximal foraminal compression tests to assess for radiating symptoms)
  • severe recent head trauma
  • acute exacerbations within the past 3 months
  • known cervical disc problems
  • surgical fusions within the cervical spine
  • highly acute symptoms
  • a positive valsalva test
  • seizure disorder
  • analgesics
  • muscle relaxants
  • medications with effects on the musculoskeletal system
  • chiropractic manipulation within 48 hours of the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Logan University, College of Chiropractic

Chesterfield, Missouri, 63017, United States

RECRUITING

Central Study Contacts

Mary Unger-Boyd, DC

CONTACT

636-230-2100mary.unger-boyd@logan.edu

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 21, 2008

First Posted

August 25, 2008

Study Start

July 1, 2008

Primary Completion

October 1, 2008

Study Completion

October 1, 2008

Last Updated

August 25, 2008

Record last verified: 2008-08

Locations

US(1)