The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial
Primary Purpose
Rotator Cuff Tears, Surgery, Pain, Postoperative
Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Slumber Curve sleep aid
Sponsored by
About this trial
This is an interventional supportive care trial for Rotator Cuff Tears
Eligibility Criteria
Inclusion Criteria:
• Any male or nonpregnant female aged 18 years or older with a full-thickness rotator cuff tear undergoing rotator cuff repair surgery
Exclusion Criteria:
- Patients who receive workers' compensation benefits
- Patients with irreparable tears
- Patients undergoing revision surgery
- Patients with concomitant severe glenohumeral arthritis or concurrent adhesive capsulitis
- Sleep apnea disorder or other diagnosed sleep disorder
- Neuropsychiatric disease
- Use of sleep medication
- Prior shoulder surgery
- Rotator cuff arthropathy with pseudo paralysis
- Acute fractures involving the proximal humerus or shoulder girdle
Sites / Locations
- UAB Hospital Highlands
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Slumber Curve Group
Normal Sleep Routine Group
Arm Description
Patients receiving Slumber Curve sleep aid for management of pain and sleep quality following rotator cuff repair.
Patients not receiving sleep aid.
Outcomes
Primary Outcome Measures
Fitbit Sleep Data - Time spent awake, restless, and asleep
Estimates of time spent awake, restless, and asleep will be assessed. All three measures will be recorded in minutes. Restless sleep indicates movement, and excessive movement will indicates time spent awake.
Fitbit Sleep Data - Sleep Stages
Sleep stages are estimated by utilizing movement and heart rate variability. Sleep stages are categorized into light sleep, deep sleep, and REM. Collective time spent in each stage will be recorded in minutes.
Pittsburgh Sleep Quality Index (PSQI)
The PSQI tracks sleep disturbances over time and includes seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, sleeping medications, and daytime dysfunction. Total of 21 points. Scores of less than 5 indicate adequate sleep. Scores of greater than 5 indicate poor sleep.
Visual Analog Scale (VAS)
Pain score, 0-10, 10 is best outcome
Single Assessment Numeric Evaluation (SANE)
Function score, 0-100%, 100% is best outcome
Postoperative Oral Morphine Equivalents
Oral morphine equivalents of all opioid-containing medications received
Simple Shoulder Test (SST)
Function score. Higher score indicates greater function.
Secondary Outcome Measures
Full Information
NCT ID
NCT04774965
First Posted
February 24, 2021
Last Updated
July 5, 2023
Sponsor
University of Alabama at Birmingham
Collaborators
Eight28, LLC
1. Study Identification
Unique Protocol Identification Number
NCT04774965
Brief Title
The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial
Official Title
The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 30, 2024 (Anticipated)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
February 1, 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
Eight28, LLC
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to investigate the effects of a novel sleep aid known as SlumberCurve™, which serves as an adjustable form of a wedge pillow, on sleep quality and pain management following rotator cuff repair. The researchers hypothesize that SlumberCurve™ will significantly improve sleep quality and reduce night-time pain.
Detailed Description
Poor sleep quality is prevalent among patients undergoing rotator cuff repair surgery, and negatively affects the potential for proper healing. Without adequate sleep, the production of anabolic steroids and inflammatory cytokines are diminished. These anabolic steroids and inflammatory cytokines play a key role in postoperative healing, resulting in adequate pain regulation and increased patient satisfaction. Therefore adequate sleep quality is important not only for quality of life, but for postoperative healing. A recent systematic review revealed that some studies reported varying degrees in both the time and magnitude of change in return to adequate sleep quality following rotator cuff repair. This study hopes to address this gap in the literature by investigating a novel sleep aid, SlumberCurve, and its effect on sleep quality and night-time pain relief. SlumberCurve is a Class I Medical Device and is currently advocated to relieve tension and diminish pain in patients undergoing rotator cuff repair surgery. The device provides adjustable elevation of the torso as well as concave positioning, placing the shoulder in a more forward position. This novel sleep aid has the potential to increase sleep quality, and therefore enhance both patient satisfaction and postoperative recovery from rotator cuff repair surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tears, Surgery, Pain, Postoperative
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Slumber Curve Group
Arm Type
Experimental
Arm Description
Patients receiving Slumber Curve sleep aid for management of pain and sleep quality following rotator cuff repair.
Arm Title
Normal Sleep Routine Group
Arm Type
No Intervention
Arm Description
Patients not receiving sleep aid.
Intervention Type
Device
Intervention Name(s)
Slumber Curve sleep aid
Intervention Description
Patients who undergo rotator cuff repair and have been consented and randomized to the experimental group will be given a Slumber Curve sleep aid to be used during sleep. Each device will be numbered and recorded in the patient's REDCap entry for future reference if needed. Following administration of the Slumber Curve, patients will be given instructions on how to use the sleep aid while sleeping, and will be asked to use Slumber Curve nightly.
Primary Outcome Measure Information:
Title
Fitbit Sleep Data - Time spent awake, restless, and asleep
Description
Estimates of time spent awake, restless, and asleep will be assessed. All three measures will be recorded in minutes. Restless sleep indicates movement, and excessive movement will indicates time spent awake.
Time Frame
90 days
Title
Fitbit Sleep Data - Sleep Stages
Description
Sleep stages are estimated by utilizing movement and heart rate variability. Sleep stages are categorized into light sleep, deep sleep, and REM. Collective time spent in each stage will be recorded in minutes.
Time Frame
90 days
Title
Pittsburgh Sleep Quality Index (PSQI)
Description
The PSQI tracks sleep disturbances over time and includes seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, sleeping medications, and daytime dysfunction. Total of 21 points. Scores of less than 5 indicate adequate sleep. Scores of greater than 5 indicate poor sleep.
Time Frame
90 days
Title
Visual Analog Scale (VAS)
Description
Pain score, 0-10, 10 is best outcome
Time Frame
90 days
Title
Single Assessment Numeric Evaluation (SANE)
Description
Function score, 0-100%, 100% is best outcome
Time Frame
90 days
Title
Postoperative Oral Morphine Equivalents
Description
Oral morphine equivalents of all opioid-containing medications received
Time Frame
90 days
Title
Simple Shoulder Test (SST)
Description
Function score. Higher score indicates greater function.
Time Frame
90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• Any male or nonpregnant female aged 18 years or older with a full-thickness rotator cuff tear undergoing rotator cuff repair surgery
Exclusion Criteria:
Patients who receive workers' compensation benefits
Patients with irreparable tears
Patients undergoing revision surgery
Patients with concomitant severe glenohumeral arthritis or concurrent adhesive capsulitis
Sleep apnea disorder or other diagnosed sleep disorder
Neuropsychiatric disease
Use of sleep medication
Prior shoulder surgery
Rotator cuff arthropathy with pseudo paralysis
Acute fractures involving the proximal humerus or shoulder girdle
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kyle D Paul, BS
Phone
2053329804
Email
kylepaul@uab.edu
Facility Information:
Facility Name
UAB Hospital Highlands
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35205
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
33447619
Citation
Kunze KN, Movasagghi K, Rossi DM, Polce EM, Cohn MR, Karhade AV, Chahla J. Systematic Review of Sleep Quality Before and After Arthroscopic Rotator Cuff Repair: Are Improvements Experienced and Maintained? Orthop J Sports Med. 2020 Dec 29;8(12):2325967120969224. doi: 10.1177/2325967120969224. eCollection 2020 Dec.
Results Reference
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The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial
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