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Impact of Day-to-Day events on Pain Management Program Outcomes: A Feasibility Study.

Not Applicable
Conditions
Chronic pain
Placebo effect
Nocebo effect
Anaesthesiology - Pain management
Mental Health - Studies of normal psychology, cognitive function and behaviour
Registration Number
ACTRN12624000071527
Lead Sponsor
Dr Vidya Shirumalla
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

•All patients aged 18 years and above presenting for CALM group program run by Central Coast Integrated Pain Service over the study period.

Exclusion Criteria

1. Refusal to consent
2. Poor literacy
3. Learning or behavioural issues
4. Other sensory barrier-visual, auditory etc
5. No or limited access to internet, poor phone connection eg remote regions.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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