NCT04749420

Brief Summary

The purpose of this study was to investigate adaptation, validity, and reliability of the Turkish version of the Cervical Radiculopathy Impact Scale (CRIS).

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
105

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2021

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

February 7, 2021

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 11, 2021

Completed
18 days until next milestone

Study Start

First participant enrolled

March 1, 2021

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2022

Completed
Last Updated

May 4, 2021

Status Verified

May 1, 2021

Enrollment Period

1.5 years

First QC Date

February 7, 2021

Last Update Submit

May 1, 2021

Conditions

Cervical RadiculopathyCervical Radicular PainCervical RadiculitisCervical Root Syndrome

Keywords

Cervical radiculopathyReliabilityValidityCross-cultural adaptation

Outcome Measures

Primary Outcomes (1)

  • Cervical Radiculopathy Impact Scale (CRIS)

    Cervical Radiculopathy Impact Scale was designed to evaluate measurement of symptoms and limitations in individuals with cervical radiculopathy.

    12 minutes

Study Arms (1)

Patients group

Individuals with cervical radiculopathy

Other: Survey study

Interventions

Survey studyOTHER

Cervical Radiculopathy Impact Scale (CRIS) will be applied

Patients group

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The study population will consist of individuals with cervical radiculpathy symptoms, diagnosis, and chronic pain on cervical spine region.

You may qualify if:

  • Individuals with radiculopathy symptoms and diagnosis.

You may not qualify if:

  • Having another neck disorder other than radiculopathy,
  • History of cervical spine surgery,
  • Corticosteroid injection to cervical spine in the past 3 months,
  • Having neurological and cognitive disorders.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Halime ARIKAN

Ankara, None Selected, 06490, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Radiculopathy

Interventions

Longitudinal Studies

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System Diseases

Intervention Hierarchy (Ancestors)

Cohort StudiesEpidemiologic StudiesEpidemiologic Study CharacteristicsEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Halime ARIKAN, MSc.

CONTACT

+90 546 576 51 32halimearikan92@gmail.com

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

February 7, 2021

First Posted

February 11, 2021

Study Start

March 1, 2021

Primary Completion

September 1, 2022

Study Completion

September 1, 2022

Last Updated

May 4, 2021

Record last verified: 2021-05

Data Sharing

IPD Sharing
Will share
Shared Documents
CSR

Locations

TU(1)