Manual Therapy, Exercise and Traction for Patients With Cervical Radiculopathy: A RCT

NCT ID: NCT00695006

Last Updated: 2008-06-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

81 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-09-30

Study Completion Date

2008-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To date, optimal strategies for the management of patients with Cervical Radiculopathy (CR) remain elusive. The purpose of this study was to compare the effects of manual therapy, exercise, and cervical traction to manual therapy, exercise, and sham traction on pain, function and disability in patients with CR.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cervical Radiculopathy

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

manual therapy, cervical traction, cervical radiculopathy

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

II

Sham Traction

Group Type SHAM_COMPARATOR

Sham Traction

Intervention Type OTHER

Traction \<5lbs

I

Traction

Group Type ACTIVE_COMPARATOR

Traction

Intervention Type OTHER

Standard supine intermittent traction

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Sham Traction

Traction \<5lbs

Intervention Type OTHER

Traction

Standard supine intermittent traction

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 3 of 4 positive on CPR, 18-70yrs

Exclusion Criteria

* history of previous cervical or thoracic spine surgery
* bilateral upper extremity symptoms
* signs or symptoms of UMN disease
* medical "red flags"(tumor, fracture, rheumatoid arthritis, osteoporosis, prolonged steroid use)
* cervical spine injections (steroidal) in the past two weeks
* current use of steroidal medication prescribed for their radiculopathy symptoms
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Rocky Mountain University of Health Professions

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Advance Rehab

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ian A Young, PT

Role: PRINCIPAL_INVESTIGATOR

Advance Rehab at Fredericksburg Orthopaedics

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Advance Rehab at Fredericksburg Orthopaedics

Fredericksburg, Virginia, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

5388642

Identifier Type: -

Identifier Source: org_study_id