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CompletedNCT02565394OR-STRETCHUpdated Feb 13, 2018

Microbreaks in the OR to Mitigate High Physical and Mental Demands

An interventional study of Micro Break with Dynamic Exercise Activities in Attention Concentration Difficulty, Neck Pain and Back Pain, sponsored by Mayo Clinic. Completed at 3 sites in United States. Open to participants aged 22 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-02-13.

Sponsored by Mayo Clinic · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Jan 2015, registered Aug 2015).
Phase
Not applicable
Study type
Interventional
Enrollment
8
Allocation
Non-randomized
Ages
22 Years and older
Sex
All
01

Study summary

Will targeted intraoperative exercises performed by surgeons during surgery, mitigate high physical and mental demands while enhancing performance during surgical procedures?

Read the detailed description

This study will compare the efficacy of incorporating dynamic exercises into the surgical procedure, to determine if the exercise intervention will decrease surgeon's perceived physical discomfort and fatigue and enhance self-reported performance during surgical procedures. All attending surgeons (Cardiothoracic, Colon and Rectal, General, Gynecology and Obstetrics, Ophthalmic, Orthopedic, Otolaryngology-Head and Neck, Neurology, Urology, Plastic and Maxillofacial, Rural, Urology, Thoracic and Vascular ) or surgeons in training that are board certified or board eligible, performing open or minimally invasive surgery within the scope of their practice in the house of surgery at Mayo Clinic Rochester, Arizona and Florida will be eligible to participate. Surgeons who have provided informed consent to participate will be asked to complete a preliminary baseline survey that will provide information regarding baseline participant characteristics and demographics.

The intervention is a web based application which will include a short video with verbal cues, available on computers in the Operating Rooms (ORs). This video will lead surgeons through the stretch exercises and include a timer to remind them when it is time to stretch. They will be able to set the time interval between stretches (between 20-55 minutes) and may activate a snooze on the timer to postpone the stretch to a more opportune time during the procedure. The stretches can be performed without breaking scrub, in the sterile field and can be completed in approximately 1 minute.

Surgeons will be asked to participate in this study for approximately 12 weeks , completing a baseline survey and three end of day surveys. They may use the intervention as much or as little as they choose during their participation, and will be free to use the application following study participation. The web application does track participant use, providing date and time stamps to enable the research team to track surgeon web app utilization. The application will also record how often the "snooze" was used to delay a stretch, or end stretches. After surgeons have accessed the web application, they will receive an email with a quick survey about their experiences with stretches, to assess the impact of the web app.

02

Conditions studied

  • Attention Concentration Difficulty
  • Neck Pain
  • Back Pain
  • Shoulder Pain
  • Fatigue
03

In context

Shoulder Pain

707 studies on the registry are indexed under Shoulder Pain; 152 are open to participants now.

This study's enrollment of 8 is below the median of 60 across 561 interventional studies indexed under Shoulder Pain.

Browse Shoulder Pain studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
22 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Attending surgeons (Cardiothoracic, Colon and Rectal, General, Gynecology and Obstetrics, Ophthalmic, Orthopedic, Otolaryngology-Head and Neck, Neurology, Urology, Plastic and Maxillofacial, Rural, Urology, Thoracic and Vascular ) or surgeons in training that are board certified or board eligible, performing open or minimally invasive surgery within the scope of their practice in the house of surgery at Mayo Clinic Rochester
  2. Over the age of 21
  3. As feasible, equal numbers of males, females and minorities
  4. Performing greater than 50% of the surgery

Exclusion criteria

Exclusion Criteria:

  1. Participants who are visibly unwell or report being unwell at time of study
  2. Participants unable to devote the minimum time required to complete study procedures
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
8 participants (actual)

Study arms

  • Experimental
    Micro-Break with Dynamic Activity

    Micro Break with web based application of a video to lead surgeons through dynamic exercise activities

    Other: Micro Break with Dynamic Exercise Activities

  • No intervention
    Comparator

    A baseline survey will be completed following a surgical day with no dynamic activities

Interventions

  • OtherMicro Break with Dynamic Exercise Activities

    Surgeons may elect to activate a web application (video) and perform targeted intraoperative exercises.

06

What researchers measure

Primary outcomes

  1. Decrease in surgeon's perceived physical discomfort and fatigue following surgeries where the dynamic exercises were performed as measured by questionnaire

    Time frame: baseline to 12 weeks

07

Study locations

3 sites
  • Mayo Clinic in Arizona
    Scottsdale, Arizona 85259, United States
  • Mayo Clinic in Florida
    Jacksonville, Florida 32224, United States
  • Mayo Clinic in Rochester
    Rochester, Minnesota 55905, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02565394
Lead sponsor
Mayo Clinic
Responsible party
Susan Hallbeck, Ph.D. (Senior Associate Consultant II, Mayo Clinic) — Principal investigator
First posted
Oct 1, 2015
Start date
Jan 2, 2015
Primary completion
Nov 6, 2017
Completion
Nov 6, 2017
Last update
Feb 13, 2018

Study contacts

Susan Hallbeck, PhD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2018. You cannot join it, but the record below documents what was studied.

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