Pain in America: A Randomized Controlled Trial

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-31

Study Completion Date

2018-04-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Orthopaedic Related Pain (Musculoskeletal Pain)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Control

This group will receive a 10 minute discussion

Group Type ACTIVE_COMPARATOR

Control

Intervention Type BEHAVIORAL

This group will receive a standardized 10 minute discussion.

Intervention

This group will receive a 10 minute standardized discussion

Group Type ACTIVE_COMPARATOR

Intervention

Intervention Type BEHAVIORAL

This group will receive a standardized 10 minute discussion

Interventions

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Control

This group will receive a standardized 10 minute discussion.

Intervention Type BEHAVIORAL

Intervention

This group will receive a standardized 10 minute discussion

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No