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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02676141
Other study ID # 2015-00068
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date February 10, 2019

Study information

Verified date February 2019
Source Balgrist University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates if the German Version of the NDI is sensitive to change over time.


Description:

Chronic neck pain patients will be asked to participate in the study.

The participants are asked to fill out the NDI at the beginning of the study and after seven weeks. Additionally the participants will fill out the PGIC.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date February 10, 2019
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Chronic neck pain

- over 18 years old

- informed consent

- able to speak, write and read German.

Exclusion Criteria:

- Any problems that may exclude Manual Therapy treatment of the cervical spine e.g fractures

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Manual Therapy
The treatment the patients receive is not specifically set up for the study. Participants will already be seeing a practitioner before the participants are included in the study.

Locations

Country Name City State
Switzerland Balgrist University Hospital Zurich

Sponsors (2)

Lead Sponsor Collaborator
Balgrist University Hospital Maastricht University

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of the German Version of the Neck Disability Index (NDI-G) Questionnaire to evaluate the subjective restriction of the participants Change from Baseline to seven weeks
Secondary Patient's Global Impression of Change Scale (PGIC) Questionnaire measuring the change of the patient. Seven weeks after the baseline measurement