NCT07656285

Recruiting

Comparison of Immediate Changes in Cervical Range of Motion ...

Missouri State University Source

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Other study identifiers

Sponsor study identifier

IRB-FY2026-122

Study Type

interventional

Estimated enrollment

128

Locations

1 country

Sites

1

Timeline

Study Start

June 12, 2026

Actual (reported)

Primary Completion

September 28, 2026

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

September 28, 2026

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Brief Summary

The purpose of this study is to compare the efficacy seated cervical extension glides vs supine downslip glides, on both cervical rotation range of motion and patient comfort. Information gathered from this study may be used to help clinicians determine the most beneficial methods of cervical mobilizations as a rehabilitation tool.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: recruiting
Estimated enrollment: 128 participants
Study completion date: September 28, 2026
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
June 11, 2026
Actual (reported)
Study Start
June 12, 2026
Actual (reported)
First Posted
June 18, 2026
Actual (reported)
Primary Completion
September 28, 2026
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
September 28, 2026
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated: June 18, 2026
Status Verified: June 2026
Last Update Submitted: June 14, 2026

Conditions

Cervical Disease

Outcome Measures

Primary Outcomes (1)

Cervical Range of Motion
Immediately following mobilization

Study Arms (2)

Cervical Downslips

EXPERIMENTAL

Other: Cervical Downslip Mobilization

Cervical Extension Glides

EXPERIMENTAL

Other: Seated Cervical Extension Glide

Interventions

Cervical Downslip MobilizationOther

Mobilization in supine on the C2-3 articular pillar in a direction that is caudal-medial-ventral.

Cervical Downslips

Seated Cervical Extension GlideOther

Mobilization of C2 on C3 in a direction that is dorsal, lateral, and caudal.

Cervical Extension Glides

Eligibility Criteria

Age18 Years - 45 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64)

You may qualify if:

healthy individuals
years of age.

You may not qualify if:

Sponsors & Collaborators

Missouri State University
Otherlead

Study Sites (1)

Missouri State University - Physical Therapy Clinic

Springfield, Missouri, 65810, United States

RECRUITING

Kim EnnisCONTACT5176143690 kwspartan10@gmail.com

MeSH Terms

Conditions

Uterine Cervical Diseases

Condition Hierarchy (Ancestors)

Uterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Diseases

Central Study Contacts

Kim Ennis, PT, ScD, OCS, FAAOMPT

CONTACT

15176143690 kwspartan10@gmail.com

Study Design

Study Type: interventional
Phase: not applicable
Allocation: RANDOMIZED
Masking: SINGLE
Who Masked: OUTCOMES ASSESSOR
Purpose: TREATMENT
Intervention Model: PARALLEL
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Assistant Professor

Study Record Dates

First Submitted

June 11, 2026

First Posted

June 18, 2026

Study Start

June 12, 2026

Actual (reported)

Primary Completion

September 28, 2026

Estimated (date passed)

Completed

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Withdrawn

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iMproving thE DIagnostics And Treatment Of ceRvical Precancer

Completed

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

current or previous history of neck pain;
cervical spine instability;
history of cervical spine surgery;
neurological issues;
contraindications to mobilization including fractures, coagulation issues, and osteoporosis

Contact the study team to confirm eligibility.

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

September 28, 2026

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated

June 18, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing: Will share
Shared Documents: STUDY PROTOCOL
Time Frame: This information will be available until statistical analysis has been completed by October 2028.
Access Criteria: Other faculty researchers including: Dalton Burke, Mike Rider, Brent Denny, Blaise Burgeois, Bob Salvatori, Hazel Anderson. They will be able to access it on a Dropbox folder that is private for anyone without access to the link.

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT07656285
Data provider: ClinicalTrials.gov
Source updated: 2026-06-18
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:29:40 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (2)

Cervical Downslips

Cervical Extension Glides

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Central Study Contacts

Study Design

Study Record Dates

Data Sharing

Source record

Locations