Prospective Trial on Noise Reduction in Surgical Operating Theaters

Sponsor
Hannover Medical School (Other)
Overall Status
Completed
CT.gov ID
NCT01612754
Collaborator
University of Zurich (Other), Technische Universität Dresden (Other)
16
1
3
19
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Study Details

Study Description

Brief Summary

Aim of Study: Adverse effects from noise pollution in operation theatres have been throughly demonstrated. We assessed the impact of a noise reduction program in paediatric surgery.

Methods: A prospective controlled study on 156 operations performed by 16 surgeons was conducted. The sound levels before and after a noise reduction program based on education, rules and technical devices (Sound Ear tm) were assessed. Endpoints were spatially resolved sound levels matched by the surgeon's biometric (saliva cortisol, electrodermal activity) and behavioural stress responses (questionnaires). These were correlated with mission protocols and NoiSeQ for individual noise sensitivity.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Noise reduction work place rules
  • Behavioral: Presence of an examiner in the concerned theatre
N/A

Detailed Description

We recorded median noise levels in the control vs. interventional group including the count of peak events with different tresholds.

Three phases were conducted: 1. Reference group/phase I 2. Control group/phase II The full data set was recorded by a research clerk present in theatre however all staff were left unaware of the study purpose 3. Intervention group/phase III. The intervention consisted of a panel of work rules including mainly communication regulations (only conversations concerning the current case were allowed, no in and out during surgery, mobile phone ban etc.. Measures were backed by intervention conferences, posters and pictograms. .

A wear off-effect was sought after . Biometrically, we analyzed the surgeon's pre- to postoperative rise in cortisol and the proportion of the surgeon's electrodermal potentials of >15µS indicating severe stress. Intra-team communication, a decrease in disturbing conversations and sudden noise peaks were investigated and correlated with the individual noise sensitivity determined by the noise Q questionnaire.

Study Design

Study Type:
Interventional
Actual Enrollment :
16 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Noise Reduction Programme by Work Rules and Technical Devices (i.e.SoundEar-TM)for Surgical Theathres
Study Start Date :
Sep 1, 2010
Actual Primary Completion Date :
Nov 1, 2011
Actual Study Completion Date :
Apr 1, 2012

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Reference group - cloaked noise meters

Reference group or phase 1 Theatre equipped with multiple sound meters disguised as CO2 meter for sound probing in the absence of a research clerk with personnel completely unaware of sound measurements.

Sham Comparator: Control Noise AND Stress measurements

Control Group - Phase 2 No intervention but research clerk is present in theatre to protocoll the operation and test for stress by collecting saliva cortisol and probing electrodermal activity

Behavioral: Presence of an examiner in the concerned theatre
Research Clerk present in theatre, writes on note pad.

Experimental: Noise Reduction Intervention Group

Intervention Group - Phase 3 A panel of noise reduction measures (staff workplace rules, technical devices as optical noise warners, optical telephones) is put into effect. Surgeons are monitored by biometry, psychometry and the outcome.

Behavioral: Noise reduction work place rules
Information conferences for all theatre staff (100%)on the detrimal effects of high noise levels in the operating theatre. Issue of "workplace rules" on handouts and poster on theatre doors: Ban of all mobile phones from theatre. Only conversations about the ongoing case are allowed. No restocking etc. during an operation and no work in this operating room concerning other patients (e.g. later on the list). Turnig of of unnecessary suckers, warming devices etc. . No in and out during the procedure. Technical: Sound Ears (TM, Sound Ear A.S. Copenhagen, Denmark) taped to all 4 Walls. Optical Telephones.
Other Names:
  • Sound Ears (TM, Sound Ear A.S. Copenhagen, Denmark)
  • Outcome Measures

    Primary Outcome Measures

    1. Noise level (dB(A)) in the operation room at the surgeon's place [continous during operation]

      noise levels are sampled simultaneously at 4 point (surgeon, nurses 1+2 and anestesiology workplace

    Secondary Outcome Measures

    1. Surgeons intraoperative biometric and psychometric stress response [before, during and after operations]

      Surgeons Cortisol Levels and Electrodermal activity are measured as he/she is submitted to questionnaires.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • all operations of our tertiary referral center practice of the regular day programme involving children from preterm babies up to children of 16 years of age including emergencies at regular hours with a duration of > 20 mins and < 5 hours
    Exclusion Criteria:
    • After hour emergency surgery

    • Pediatric surgery cardiac cases

    • surgeries <20 mins/>5hrs

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Pediatric Surgery Department Hannover Lower Saxony Germany 30625

    Sponsors and Collaborators

    • Hannover Medical School
    • University of Zurich
    • Technische Universität Dresden

    Investigators

    • Principal Investigator: Carsten R Engelmann, MD, PhD, Hannover Medical School, Germany

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Carsten Engelmann, Oberarzt Kinderchirurgie, Hannover Medical School
    ClinicalTrials.gov Identifier:
    NCT01612754
    Other Study ID Numbers:
    • SA 02
    First Posted:
    Jun 6, 2012
    Last Update Posted:
    Jun 6, 2012
    Last Verified:
    Jun 1, 2012
    Keywords provided by Carsten Engelmann, Oberarzt Kinderchirurgie, Hannover Medical School

    Study Results

    No Results Posted as of Jun 6, 2012