Patient Education for Patients With Back Pain Referred to Physical Therapy

NCT ID: NCT02648373

Last Updated: 2016-01-07

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

COMPLETED

Clinical Phase

NA

Total Enrollment

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2015-10-31

Brief Summary

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The purpose of this study is to evaluate patients with low back pain who are scheduled to begin physical therapy but have not yet had their first appointment to better understand their beliefs and attitudes and to evaluate the effects of an educational session about low back pain.

Detailed Description

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The investigators will conduct a randomized trial to examine the effectiveness of a patient education session provided prior to beginning physical therapy on outcomes of usual physical therapy for acute/sub-acute low back pain patients. The study compares two groups, one group will be treated with usual physical therapy with no pre-treatment education and the other group will also receive the pre-treatment. Patients will be followed after 6 weeks and 3 months. Physical therapy care is left to the discretion of the physical therapist in conjunction with the patient. Outcomes will include pain and disability, and patients attitude and believes (pain catastrophizing, fear avoidance behavior). The overall hypothesis is that the additional educational treatment may address and improve pain, disability and fear.

Conditions

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Low Back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Education

Patients receive an educational video about low back pain based on the Consumer Reports Choosing Wisely recommendation for patients with back pain to avoid early imaging and remain as active as possible. After the video the evaluator and patient discussed key themes from the video and the patient was able to ask any questions. Previously scheduled physical therapy then began with treatment at the therapist's discretion.

Group Type EXPERIMENTAL

Patient Education

Intervention Type BEHAVIORAL

An educational video was watched based on Consumer Reports Choosing Wisely patient education supporting the recommendation that imaging is not helpful early for low back pain and the best strategy is to remain as active as possible. Key themes were discussed with a physical therapist and the patient's questions were answered.

Control

Previously scheduled physical therapy was provided with treatment at the therapist's discretion. No educational intervention was provided before beginning physical therapy

Group Type ACTIVE_COMPARATOR

Control

Intervention Type OTHER

Patients receive no additional intervention. They will begin physical therapy and receive care at the therapist's discretion.

Interventions

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Patient Education

An educational video was watched based on Consumer Reports Choosing Wisely patient education supporting the recommendation that imaging is not helpful early for low back pain and the best strategy is to remain as active as possible. Key themes were discussed with a physical therapist and the patient's questions were answered.

Intervention Type BEHAVIORAL

Control

Patients receive no additional intervention. They will begin physical therapy and receive care at the therapist's discretion.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Chief complaint of non-specific low back pain scheduled to receive outpatient physical therapy
* age 18-60
* duration of current symptoms \< 8weeks
* referred to physical therapy from a non-surgeon provider
* no treatment received for low back pain in past year other than physician office visits.

Exclusion Criteria

* Diagnosis provided by the referral source indicating a specific pathoanatomical source for LBP including fracture, spondylolesthesis, ankylosing spondylitis, radiculopathy
* any red flags in the patient's general medical screening questionnaire (i.e. tumor, metabolic diseases etc.).
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Utah

OTHER

Sponsor Role lead

Responsible Party

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Julie Fritz

Ph.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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The University of Utah Healthcare System

Salt Lake City, Utah, United States

Site Status

Countries

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United States

Other Identifiers

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IRB00072901

Identifier Type: -

Identifier Source: org_study_id

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