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NCT02892032 Clinical Trial

Attention Training Trial

Chronic Pain Clinical Trial

Official title:
Mobile Based Attention Bias Modification Training for Chronic Pain

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02892032
Other study ID # e2016-240
Secondary ID
Status Withdrawn
Phase N/A
First received August 30, 2016
Last updated January 9, 2018
Start date August 2016
Est. completion date August 2020

Study information
Verified date January 2018
Source York University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to examine the effects of smartphone-based Attention-Bias Modification Training (ABMT) in chronic pain participants.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date August 2020
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- existing chronic pain condition

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Attention Modification Training
Subjects are taught to disengage attention from a certain stimuli
• No Attention Modification Training
Subjects are exposed to two stimuli, but attention is not manipulated in any way

Locations
Country Name City State
Canada York University Toronto Ontario

Sponsors (1)
Lead Sponsor Collaborator
York University

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain intensity questionnaire (numerical pain rating scale) 1 hour
Secondary pain interference questionnaire (pain interference scale) 1 hour
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