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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02690597
Other study ID # 12 560 07
Secondary ID 2013-A00451-44
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date December 2016

Study information

Verified date November 2018
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Screening of anxiogenic part of pain is an imperative during a medical pain consultation. The actual tools for evaluation of this specific part are complex and time consuming.

To date, it lacked a reliable and reproductive tool to quickly evaluate anxiety of patient in pain. The purpose of this study is to demonstrate the pertinence and validity of anxiety analogic visual scale by comparison with the actual reference the self-assessment questionnaire State Trait Inventory Anxiety Y-A form.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Signed and dated informed consent

- Male or female aged from = 18 years old

- Perfect patient ability to understand and write French

- Patient with a pain threshold permitting a initial medication free consultation and completion of anxiety surveys.

Exclusion Criteria:

- Inability of patient to understand the study procedures and thus inability to give informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Anxiety visual analog scale
Anxiety visual analog scale is a test of evaluation of anxiety done by the patient, this scale do not include number and the patient have to place a coloured marker at the level indicating his anxiety feeling

Locations

Country Name City State
France CHU Rangueil Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of pertinence of anxiety analogic visual scale in systematic use as assessed by anxiety levels obtained with State Trait of anxiety Y-A form score The patient's inclusion take place during the only study participation day of the patient Baseline
Primary Evaluation of validity of anxiety analogic visual scale in systematic use as assessed by anxiety levels obtained with State Trait of anxiety Y-A form score The patient's inclusion take place during the only study participation day of the patient Baseline
Primary Evaluation of pertinence of anxiety analogic visual scale in systematic use as assessed by anxiety levels obtained with anxiety analogic visual scale score The patient's inclusion take place during the only study participation day of the patient Baseline
Primary Evaluation of validity of anxiety analogic visual scale in systematic use as assessed by anxiety levels obtained with anxiety analogic visual scale score The patient's inclusion take place during the only study participation day of the patient Baseline
Secondary Evaluation of pain consultation impact on anxiety part of pain as assessed by anxiety levels obtained with State Trait of anxiety Y-A form score The patient's inclusion take place during the only study participation day of the patient Baseline
Secondary Evaluation of pain consultation impact on anxiety part of pain as assessed by anxiety levels obtained with anxiety analogic visual scale score The patient's inclusion take place during the only study participation day of the patient Baseline
Secondary Evaluation of clinical utility of anxiety analogic visual scale in nursing care as assessed by anxiety levels obtained with State Trait of anxiety Y-A form score The patient's inclusion take place during the only study participation day of the patient Baseline
Secondary Evaluation of clinical utility of anxiety analogic visual scale in nursing care as assessed by anxiety levels anxiety analogic visual scale score The patient's inclusion take place during the only study participation day of the patient Baseline
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