Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02710695
Other study ID # 16-026
Secondary ID
Status Terminated
Phase N/A
First received March 12, 2016
Last updated April 24, 2018
Start date March 2016
Est. completion date April 2018

Study information

Verified date April 2018
Source University of Missouri, Kansas City
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Each day orthopaedic surgeons worldwide treat patients with musculoskeletal pain. But little evidence exists about orthopaedic patient understanding of the common methods of managing musculoskeletal pain. Therefore, it is our aim to determine which discussion method best improves patient comprehension of common methods of managing pain.


Recruitment information / eligibility

Status Terminated
Enrollment 50
Est. completion date April 2018
Est. primary completion date April 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients who are new to a discussion about the common methods of managing musculoskeletal pain, over the age of 18, native English speakers

Exclusion Criteria:

- Patient with a previous orthopaedic surgery or musculoskeletal pain consultation, patients without the capacity to give consent, chronic narcotic users. Patients with a severe mental, visual, auditory or tactile impairment.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Control
This group will receive a standardized 10 minute discussion.
Intervention
This group will receive a standardized 10 minute discussion

Locations

Country Name City State
United States UMKC Department of Orthopaedic Surgery Kansas City Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Missouri, Kansas City

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Nkem Musculoskeletal Pain Management Comprehension Test "NMPMCT" Validated Questionnaire 15 minutes
Secondary Surveys 5 minutes