NCT00172237

Brief Summary

Specific aims of this project were as follows:

  1. 1.To investigate the eye-head coordination of patients with cervical spine degeneration.
  2. 2.To investigate the relationship of these impairment measurements (range of motion, muscle power, proprioception, sensory threshold, eye-head coordination) and functional outcome (neck disability index, quality of life evaluation).
  3. 3.To develop a computer assistant device and software for the proprioceptive training and eye-head coordination.
  4. 4.To provide a treatment and prevention program emphasized on proprioception treatment and coordination for employee with neck-shoulder complaints.

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
80

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2009

Shorter than P25 for all trials

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

September 12, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 15, 2005

Completed
4.2 years until next milestone

Study Start

First participant enrolled

December 1, 2009

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2010

Completed
Last Updated

January 29, 2010

Status Verified

January 1, 2010

First QC Date

September 12, 2005

Last Update Submit

January 28, 2010

Conditions

Spinal Diseases

Keywords

eye-head coordinationproprioceptioncervical spine with degenerative diseasedegenerated cervical spine

Eligibility Criteria

Age45 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

45-64 year-old healthy adults and adults with neck pain

You may qualify if:

  • Group one: participants without degenerated disease in cervical spine
  • Group two: participants with degenerated disease in cervical spine

You may not qualify if:

  • Grade III, IV degenerated cervical spine

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

School and Graduate Institute of Physical Therapy

Taipei, 100, Taiwan

RECRUITING

MeSH Terms

Conditions

Spinal Diseases

Condition Hierarchy (Ancestors)

Bone DiseasesMusculoskeletal Diseases

Study Officials

  • Shwu-Fen Wang, Ph.D

    School and Graduate Institute of Physical Therapy, National Taiwan University

    STUDY CHAIR

Central Study Contacts

Shwu-Fen Wang, Ph.D

CONTACT

886-2-23123456sfwang@ntu.edu.tw

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 12, 2005

First Posted

September 15, 2005

Study Start

December 1, 2009

Study Completion

July 1, 2010

Last Updated

January 29, 2010

Record last verified: 2010-01

Locations

TW(1)