Actively Recruiting

Age: 18Years - 75Years
All Genders
NCT06084520

Translation and Validation of the COMM and ASI-SR

Led by Uppsala University · Updated on 2024-05-10

400

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

Sponsors

U

Uppsala University

Lead Sponsor

T

The Kamprad Family Foundation for Entrepreneurship, Research & Charity

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to translate the COMM (Current opinion misuse measure) form and validate it using the ASI-SR (Addiction severity score-self report)in a Swedish population of pain patients treated with opioids. The secondary aim is to investigate acceptability of the instrument in a Swedish population of pain patients with long-term opioid treatment (LOT). The tertiary aim is to investigate the prevalence of alcohol and illicit substance use in a Swedish population of pain patients with LOT.

CONDITIONS

Official Title

Translation and Validation of the COMM and ASI-SR

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 75 years
  • Patients with long-term, non-cancer-related pain lasting more than 3 months and occurring at least 3 days a week
  • Intervention group: opioid treatment for at least 1 month during the last 6 months
  • Control group: no opioid treatment at inclusion and during the last 3 months
  • Fluent in spoken and written Swedish
Not Eligible

You will not qualify if you...

  • Ongoing diseases or conditions that prevent the patient from completing the study as assessed by a doctor
  • Serious cognitive disorder making it impossible to answer questions
  • Ongoing or treated cancer in the last 10 years
  • Insufficient knowledge of Swedish

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Multidisciplinary Pain Center

Uppsala, Uppland, Sweden, 75185

Actively Recruiting

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Research Team

L

Lenka Katila, MD

CONTACT

R

Rolf Karlsten, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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