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The Influence of a Protein Nutrition Beverage on Exercise-based Rehabilitation Outcomes in Individuals With Spine Pain.

Primary Purpose

Low Back Pain

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Protein supplement
Sponsored by
Kamshad Raiszadeh, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring Protein Supplement, Exercise-based Rehabilitation

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Seeking treatment for spinal conditions, pain or for the prevention of future injury
  • Ability to consume protein shake and follow storage, timing and preparation instructions
  • Indicated by a qualified health care provider to safely participate in an exercise-based rehabilitation program
  • Ability to read and comprehend the English language

Exclusion Criteria:

  • Certain medical conditions, diagnosis, physical or psychological or physical exam finding that precludes participation, medications, or contraindications for protein supplement

    • Individuals who are determined by their health care provider to be contraindicated for participation in an exercise-based rehabilitation program
    • Individuals with food allergies to animal based products, nuts, and/or eggs
    • Individuals with consumption preferences omitting non-vegan or vegetarian products
    • Taking protein supplements already
    • History of severe liver disorder
    • History of Kidney disorder
    • History of diabetes
    • History of Gastrointestinal malabsorption
    • History of Parathyroid gland disorders
    • Pregnant, postpartum up to six months, lactating, or intention to become pregnant

Sites / Locations

  • SpineZone

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Protein Intervention Group

Control Group

Arm Description

Patients who receive the protein nutritional supplement as part of their prescribed exercise-based rehabilitation program.

Patients who receive the prescribed exercise-based rehabilitation program, without protein supplement.

Outcomes

Primary Outcome Measures

Muscle size
Change in spine extensor muscle cross sectional area (cm2)

Secondary Outcome Measures

Symptom inference - change in pain. Visual Analogue Scale (VAS), 0-100mm
Difference in VAS (in mm) between initial evaluation and endpoint
Change in disability
Difference in Oswestry Disability Index (ODI), between evaluation and end point
Patient Goal Achievement
Patient Specific Functional Scale (PSFS), 0-10 points
Change in strength (lbs*deg)
Difference in spine extension torque as measures by isokinetic dynamometer between initial evaluation and endpoint

Full Information

First Posted
March 30, 2021
Last Updated
March 16, 2022
Sponsor
Kamshad Raiszadeh, MD
Collaborators
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT04829448
Brief Title
The Influence of a Protein Nutrition Beverage on Exercise-based Rehabilitation Outcomes in Individuals With Spine Pain.
Official Title
The Influence of a Protein Nutrition Beverage on Exercise-based Rehabilitation Outcomes in Individuals With Spine Pain.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
March 16, 2022 (Actual)
Primary Completion Date
April 2026 (Anticipated)
Study Completion Date
April 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kamshad Raiszadeh, MD
Collaborators
University of California, San Diego

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
SpineZone is an innovative physical therapy program with its focus on treatment of cervical, thoracic, and lumbar conditions through the use of a multi-disciplinary, technology enabled platform. Standard physical therapy modalities including exercise-based rehabilitation as well as patient education on a healthy lifestyle (sleep, nutrition, posture) are employed as part of the standard treatment. As nutrition is a key element in modulating muscle growth and function in response to exercise, providing patients with appropriate access to nutritional supplements that meet the metabolic demands of our exercise program are potentially important to our clinical outcomes.
Detailed Description
Low back pain manifests itself clinically with pain, loss of strength, difficulty with normal posture, and decreased range of motion. In as many as 60-85% cases, LBP will become a chronic condition, requiring long term care, and even surgery. Conservative therapy is typically administered until it's no longer a viable option, after which surgical options are considered. Conservative therapy includes physical therapy, medication, steroid injections etc. Physical therapy and exercises are especially central to conservative therapy. Numerous exercise and therapy protocols have been designed with the goal to improve low back muscle strength, thereby alleviating symptoms, and potentially underlying cause of the pathology. As nutrition is a key element in modulating muscle growth and function in response to exercise, providing patients with appropriate access to nutritional supplements that meet the metabolic demands of our exercise program are potentially important to our clinical outcomes. The project specifically aims to assess the effect of ensuring adequate nutritional availability of protein, as protein shake, as part of their standard care for treatment of low back pain typically 4-12 weeks duration. In this experiment, we will compare muscle structure and health and correlate improvements with patient-specific characteristics such as demographics, medical history, medication usage, treatment expectations, and symptom severity. Subsequently, this information will enable us to gain valuable insight into physiological response of pathological tissue, and potentially, develop optimal exercise plans to maximally benefit these patients. AIMS OF THE STUDY To evaluate the adherence and compliance of patients taking a protein nutritional supplement in this patient population. To evaluate the effectiveness of protein nutritional supplementation on improving clinical outcomes. Identify patients (based on patient specific predictors who are most likely to succeed with the addition of nutritional supplementation. The goal of this project is to assess the impact of a nutritional protein supplement on clinical outcomes in individuals with spine pain. RESEARCH PARTICIPANTS We will recruit up to 100 individuals with LBP of > 3months duration that have been identified by the care providers (ie. Primary care physical, orthopaedic surgeon, or other) to be appropriate and safe for participation in a physical rehabilitation program with nutritional supplementation at SpineZone. Upon initial evaluation at the SpineZone clinic with a Physical Therapist, participants will be offered the opportunity participate in the study and may receive the protein supplement as part of their standard care. Potentially interested patients will be screened by inclusion and exclusion criteria and as such, written informed consent will be obtained from each patient. Patients will then be randomly assigned to the treatment (protein supplement) or control group (no protein supplement) and commence their prescribed rehabilitation treatment as per therapist recommendation. Individuals in the randomly assigned supplementation group will be provided the supplement and will be instructed on its use (dosage and frequency). CONSENT All guidelines for proper consenting will be observed. Consenting will be done in a private room prior to any procedures being performed. Patients will be given ample time to review the document and ask questions. All study procedures will be thoroughly explained and all questions will be answered. Patients will not be placed under any pressure to participate in the study. Consent forms will be obtained by the investigators of the study and/or the study coordinator in the SpineZone clinics. Withdrawal from the study: If the patient decides at any point to withdraw from the study, they can do so without any of the benefits to which they are entitled changing. RISK/BENEFITS RATIO The risks to the patients will be minimal. Although there is, future patients may benefit from improvements to surgical procedures and more effective rehabilitation programs which will be derived from patient outcomes. DATA PRIVACY AND CONFIDENTIALITY A confidentiality breach is a risk associated with data review research; however every measure will be instituted to ensure that patient information is kept confidential. Data analysis worksheets will be kept separate from EMR records. No subject public health information will be collected or shared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
Protein Supplement, Exercise-based Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Protein Intervention Group
Arm Type
Experimental
Arm Description
Patients who receive the protein nutritional supplement as part of their prescribed exercise-based rehabilitation program.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Patients who receive the prescribed exercise-based rehabilitation program, without protein supplement.
Intervention Type
Dietary Supplement
Intervention Name(s)
Protein supplement
Intervention Description
Protein supplement equivalent to Metagenics Ultrameal
Primary Outcome Measure Information:
Title
Muscle size
Description
Change in spine extensor muscle cross sectional area (cm2)
Time Frame
3 months, 6 months, 1 year, 2 years
Secondary Outcome Measure Information:
Title
Symptom inference - change in pain. Visual Analogue Scale (VAS), 0-100mm
Description
Difference in VAS (in mm) between initial evaluation and endpoint
Time Frame
3 months, 6 months, 1 year, 2 years
Title
Change in disability
Description
Difference in Oswestry Disability Index (ODI), between evaluation and end point
Time Frame
3 months, 6 months, 1 year, 2 years
Title
Patient Goal Achievement
Description
Patient Specific Functional Scale (PSFS), 0-10 points
Time Frame
3 months, 6 months
Title
Change in strength (lbs*deg)
Description
Difference in spine extension torque as measures by isokinetic dynamometer between initial evaluation and endpoint
Time Frame
3 months, 6 months, 1 year, 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Seeking treatment for spinal conditions, pain or for the prevention of future injury Ability to consume protein shake and follow storage, timing and preparation instructions Indicated by a qualified health care provider to safely participate in an exercise-based rehabilitation program Ability to read and comprehend the English language Exclusion Criteria: Certain medical conditions, diagnosis, physical or psychological or physical exam finding that precludes participation, medications, or contraindications for protein supplement Individuals who are determined by their health care provider to be contraindicated for participation in an exercise-based rehabilitation program Individuals with food allergies to animal based products, nuts, and/or eggs Individuals with consumption preferences omitting non-vegan or vegetarian products Taking protein supplements already History of severe liver disorder History of Kidney disorder History of diabetes History of Gastrointestinal malabsorption History of Parathyroid gland disorders Pregnant, postpartum up to six months, lactating, or intention to become pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bahar Shahidi, PT, PhD
Organizational Affiliation
UCSD Orthopedic Surgery
Official's Role
Study Director
Facility Information:
Facility Name
SpineZone
City
San Diego
State/Province
California
ZIP/Postal Code
92108
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Patient data will only be accessible to SpineZone and collaborating research partners (UCSD).

Learn more about this trial

The Influence of a Protein Nutrition Beverage on Exercise-based Rehabilitation Outcomes in Individuals With Spine Pain.

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