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Effectiveness of Biofreeze® on Shoulder Pain and In-office Exercise Performance (BFShld01)

Primary Purpose

Shoulder Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Biofreeze
Sponsored by
Sport and Spine Rehab Clinical Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Shoulder Pain

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18-64 years old
  • mechanical shoulder pain
  • candidates for conservative care

Exclusion Criteria:

  • pregnancy
  • radicular symptoms
  • not a candidate for conservative care
  • history of recent shoulder surgery

Sites / Locations

  • Sport & Spine Rehab

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Biofreeze

Control

Arm Description

Apply 5 minutes before therapy by applying a small coin sized amount to the painful area. Subjects will then complete a standard shoulder therapy program.

Subjects in this arm will complete a standard shoulder therapy program as normal, with no intervention.

Outcomes

Primary Outcome Measures

Change From Baseline of American Shoulder and Elbow Surgeons (ASES) Questionnaire at 2 Weeks
The American Shoulder and Elbow Surgeons (ASES) Questionnaire is a self-report questionnaire measuring pain and disability. It is measured from 0 to 100, 0 being completely disabled and 100 being pain free and normal function. The total score is calculated using the following equation: (10-NPRS) x 5 = __ + (5/3) x Cumulative ADL Score
Change From Baseline of Numeric Pain Rating Scale (NPRS) at 2 Weeks
The Numeric Pain Rating Scale (NPRS) is a self-report scale measuring pain. It is measured from 0 to 10, 0 being pain free and 10 being the worse imaginable pain.
Change From Baseline of American Shoulder and Elbow Surgeons (ASES) Questionnaire at 4 Weeks
The American Shoulder and Elbow Surgeons (ASES) Questionnaire is a self-report questionnaire measuring pain and disability. It is measured from 0 to 100, 0 being completely disabled and 100 being pain free and normal function. The total score is calculated using the following equation: (10-NPRS) x 5 = __ + (5/3) x Cumulative ADL Score
Change From Baseline of Numeric Pain Rating Scale (NPRS)at 4 Weeks
The Numeric Pain Rating Scale (NPRS) is a self-report scale measuring pain. It is measured from 0 to 10, 0 being pain free and 10 being the worse imaginable pain.

Secondary Outcome Measures

Full Information

First Posted
April 2, 2013
Last Updated
January 11, 2016
Sponsor
Sport and Spine Rehab Clinical Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01827306
Brief Title
Effectiveness of Biofreeze® on Shoulder Pain and In-office Exercise Performance
Acronym
BFShld01
Official Title
Effectiveness of Biofreeze® on Shoulder Pain and In-office Exercise Performance: A Preliminary Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sport and Spine Rehab Clinical Research Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Biofreeze® is a topical analgesic, frequently used in the office or given to a patient for home use as a way to mitigate pain during the course of treatment. Rehabilitative exercises are considered an important component of care for shoulder pain patients, although pain can be a limiting factor in the advancement of rehabilitation. The purpose of this study is to evaluate the addition of Biofreeze® to an in-office group of shoulder pain patients to determine its impact on pain reduction. Methods: Patients 18-64 years old with mechanical shoulder pain who are candidates for standard shoulder therapy will be randomized into two groups (N=20). The Control group (N=10) will receive standard shoulder therapy alone while the Intervention group (N=10) will receive standard shoulder therapy plus Biofreeze® just prior to initiating the in-office exercise program. Values of pain (NPRS) and disability (ASES) will be recorded at baseline, 2 weeks, and 4 weeks. Hypotheses will be addressed by repeated measures ANOVAs within and between group, time, and interaction main effects. Clinical Relevance: Progression of therapeutic exercises can be limited by pain and the associated disability. The ability to decrease shoulder pain and disability with a topical analgesic will allow health care professionals to advance patients through a therapeutic exercise program without the restriction of pain. In turn, patients will correct the underlying condition of their shoulder pain at a faster rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Biofreeze
Arm Type
Active Comparator
Arm Description
Apply 5 minutes before therapy by applying a small coin sized amount to the painful area. Subjects will then complete a standard shoulder therapy program.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Subjects in this arm will complete a standard shoulder therapy program as normal, with no intervention.
Intervention Type
Drug
Intervention Name(s)
Biofreeze
Primary Outcome Measure Information:
Title
Change From Baseline of American Shoulder and Elbow Surgeons (ASES) Questionnaire at 2 Weeks
Description
The American Shoulder and Elbow Surgeons (ASES) Questionnaire is a self-report questionnaire measuring pain and disability. It is measured from 0 to 100, 0 being completely disabled and 100 being pain free and normal function. The total score is calculated using the following equation: (10-NPRS) x 5 = __ + (5/3) x Cumulative ADL Score
Time Frame
2 weeks
Title
Change From Baseline of Numeric Pain Rating Scale (NPRS) at 2 Weeks
Description
The Numeric Pain Rating Scale (NPRS) is a self-report scale measuring pain. It is measured from 0 to 10, 0 being pain free and 10 being the worse imaginable pain.
Time Frame
2 weeks
Title
Change From Baseline of American Shoulder and Elbow Surgeons (ASES) Questionnaire at 4 Weeks
Description
The American Shoulder and Elbow Surgeons (ASES) Questionnaire is a self-report questionnaire measuring pain and disability. It is measured from 0 to 100, 0 being completely disabled and 100 being pain free and normal function. The total score is calculated using the following equation: (10-NPRS) x 5 = __ + (5/3) x Cumulative ADL Score
Time Frame
4 weeks
Title
Change From Baseline of Numeric Pain Rating Scale (NPRS)at 4 Weeks
Description
The Numeric Pain Rating Scale (NPRS) is a self-report scale measuring pain. It is measured from 0 to 10, 0 being pain free and 10 being the worse imaginable pain.
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-64 years old mechanical shoulder pain candidates for conservative care Exclusion Criteria: pregnancy radicular symptoms not a candidate for conservative care history of recent shoulder surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay Greenstein, DC
Organizational Affiliation
Sport and Spine Rehab Clinical Research Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sport & Spine Rehab
City
Rockville
State/Province
Maryland
ZIP/Postal Code
20852
Country
United States

12. IPD Sharing Statement

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Effectiveness of Biofreeze® on Shoulder Pain and In-office Exercise Performance

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