Cognitive Bias Modification for interpretation and Expectancy in Patients with Chronic Pai

Not Applicable

• Conditions: chronic pain; Musculoskeletal - Osteoarthritis; Musculoskeletal - Other muscular and skeletal disorders; Neurological - Other neurological disorders

• Registration Number: ACTRN12618001374257
• Lead Sponsor: niversity of Sydney

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-08-16
• Last Update Posted: 15 July 2019

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 220

Inclusion Criteria

Chronic pain (pain > 4/10 on more days that not over the last 3 months)
- Internet access
- Computer literacy

Exclusion Criteria

N/A. It is anticipated that the self-selecting nature of the study will exclude participants who would otherwise not be deemed appropriate (e.g. not able to use the computer due to pain, significant cognitive deficits)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Brief Pain Inventory: Intensity subscale This measure will be used to evaluate the severity of participants’ pain (BPI). It will be administered pre-training, after each subsequent (i.e. 3/4) training sessions, at follow-up point 1 (14 days post-baseline) and at follow-up point 2 (28 days post baseline). [1. pre-training 2. after each training session 3. follow-up point 1 (14 days post-baseline) [primary timepoint] 4. follow-up point 2 (28 days post-baseline) ];Brief Pain Inventory: Interference Subscale<br>This measure will be used to evaluate the severity of participants’ pain and the impact of this pain on their daily functioning (BPI). It will be administered pre-training, after each subsequent (i.e. 3/4) training sessions (x3), at follow-up point 1 (7 days post-baseline) and at follow-up point 2 (14 days post baseline).[1. pre-training 2. after each training session 3. follow-up point 1 (14 days post-baseline) [primary timepoint] 4. follow-up point 2 (28 days post-baseline) ]