MedPath

Attention Training Trial

Not Applicable
Withdrawn
Conditions
Chronic Pain
Interventions
Behavioral: No Attention Modification Training
Behavioral: Attention Modification Training
Registration Number
NCT02892032
Lead Sponsor
York University
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • existing chronic pain condition
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
No Attention Modification TrainingNo Attention Modification TrainingThere is no disengagement of attention from a target stimulus. Attention is divided equally between two stimuli on the screen.
Attention Modification TrainingAttention Modification TrainingABMT is a newly emerging intervention that trains patients to override their tendency to focus on threatening aspects of an event and to interpret events as more neutral and therefore less stressful
Primary Outcome Measures
NameTimeMethod
pain intensity1 hour

questionnaire (numerical pain rating scale)

Secondary Outcome Measures
NameTimeMethod
pain interference1 hour

questionnaire (pain interference scale)

Trial Locations

Locations (1)

York University

🇨🇦

Toronto, Ontario, Canada

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