NCT00266981

Brief Summary

The purpose of this study is to compare two techniques for treating patients with Whiplash Associated Disorders, in relation to: disability, balance, cervical pain and cervical range of motion. The hypothesis: The APOS kit treatment is more effective than the short wave therapy.

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
132

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2006

Shorter than P25 for not_applicable

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

First Submitted

Initial submission to the registry

December 19, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 20, 2005

Completed
2 months until next milestone

Study Start

First participant enrolled

March 1, 2006

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2006

Completed
Last Updated

December 20, 2005

Status Verified

December 1, 2005

First QC Date

December 19, 2005

Last Update Submit

December 19, 2005

Conditions

Whiplash Associated DisordersCervical Pain

Outcome Measures

Primary Outcomes (4)

  • neck disability score

  • neck pain score

  • balance score

  • cervical range of motion

Interventions

APOS - exercise componentDEVICE

Eligibility Criteria

Age16 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hadassah Medical Organization

Jerusalem, Israel

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Milka Donchin, MD, MPH

    School of Public Health, Hadassah Medical Organization

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Goni Meron, PTB

CONTACT

00 972 2 5335039goni_yehudai@walla.co.il

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 19, 2005

First Posted

December 20, 2005

Study Start

March 1, 2006

Study Completion

December 1, 2006

Last Updated

December 20, 2005

Record last verified: 2005-12

Locations

IL(1)