The Effect of Dream Doctors in Children Undergoing Digestive Endoscopic Procedures

October 2, 2018 updated by: Sarit Peleg, HaEmek Medical Center, Israel

The Effect of Dream Doctors in Children Undergoing Digestive Endoscopic Procedures: Physiological and Biological Assessment of Emotional and Cognitive Consequences

Background: Performance of endoscopy in children requires more patience, experience, and expertise than in adults. The anxiety of the children is related to parent's separation, loss of self-control, unknown surroundings and strange people that are taking care of them, and frequently unpleasant or even painful procedures. Painful and frightening procedures in children have been shown to result in short-term physiologic changes and long-term behavioral changes. The response to unpleasant stimuli with stress and fear may be exaggerated in children and experienced as pain. Most infants and children and many teenagers need deep sedation or light general anesthesia to complete a successful and safe procedure. Induction of general anesthesia is a stressful procedure itself. Strategies to reduce preanesthesia anxiety include pharmacologic and non-pharmacologic interventions.

However, this evidence is based mainly on self reports rather than objective measurements. Therefore, objective and non-invasive measurements to be utilized in the current study, should provide an assessment tools regardless the children's age.

Multiple studies, beginning in the 1970's, have shown that humor has many positive effects on physical and mental health and well-being. Previous investigations have reported that humor has beneficial effects on the immune system, stress related to potentially fatal illnesses, pain tolerance, and mental functions.

Dream doctors (DDs) are professional medical clowns or stage artists, who received training specifically to understand medical patient's need and to give the patient adjuvant therapy during hospital admissions or ambulatory treatment.The Israel dream doctors project, integrates professional medical clowning into the medical services provided at Israeli hospitals.Studies already proved that presence of medical clowns significantly reduces the level of anxiety during induction of anesthesia in children. Hypothesis of the study: 1) DDs lessen the level of anxiety and attention impairment in children undergoing gastroscopies. 2) DDs improve the satisfaction of children and their parents during gastroscopies.

The aim of this study is: 1) To explore the influence of DDs on the satisfaction of children and their parents undergoing gastroscopy, utilizing questioners. 2) To explore the effects of DDs on anxiety and attention of children and their parents, undergoing gastroscopies by means of GSR, startle response and pre-pulse inhibition (PPI) tests, as well as , and measuring anxiety-related biologic indices.

Study Overview

Detailed Description

The effect of Dream Doctors in children undergoing digestive endoscopic procedures: Physiological and biological assessment of emotional and cognitive consequences.

Background: Since the advent of pediatric gastrointestinal endoscopy in the early 1970's, there has been a remarkable increase in the number of diagnostic and therapeutic procedures performed in infants and children. Performance of endoscopy in children requires more patience, experience, and expertise than in adults. The anxiety of the children is related to parent's separation, loss of self-control, unknown surroundings and strange people that are taking care of them, and frequently unpleasant or even painful procedures. Painful and frightening procedures in children have been shown to result in short-term physiologic changes and long-term behavioral changes. The response to unpleasant stimuli with stress and fear may be exaggerated in children and experienced as pain. Most infants and children and many teenagers need deep sedation or light general anesthesia to complete a successful and safe procedure. Induction of general anesthesia is a stressful procedure itself. Strategies to reduce preanesthesia anxiety include pharmacologic and non-pharmacologic interventions.

However, this evidence is based mainly on self reports rather than objective measurements. Therefore, objective and non-invasive measurements to be utilized in the current study, should provide an assessment tools regardless the children's age.

Multiple studies, beginning in the 1970's, have shown that humor has many positive effects on physical and mental health and well-being. Previous investigations have reported that humor has beneficial effects on the immune system, stress related to potentially fatal illnesses, pain tolerance, and mental functions.

Dream doctors are professional medical clowns or stage artists, who received training specifically to understand medical patient's need and to give the patient adjuvant therapy during hospital admissions or ambulatory treatment. Laughter has physiological effects on different body mechanisms and it affects the cardiovascular system (decreasing heart rate and blood pressure), strengthens the immune system, and lowers level of stress hormones like Norepinephrine. Humor can also help in strengthening the bond between therapist and patient and reduce stress and anxiety and enhance recovery. The Israel dream doctors project, integrates professional medical clowning into the medical services provided at Israeli hospitals. The DDs are part of the multidisciplinary staff, principally but not only, in pediatric wards. Studies already proved that presence of medical clowns significantly reduces the level of anxiety during induction of anesthesia in children. In the pediatric ward in Afula Medical Center, the investigators have experience with DDs for preparing children to kidney scans.

Pre-Puls Inhibition PPI A computerized human startle response monitoring system (SR-HLAB STARTLE REFLEX, San Diego Instruments, San Diego, CA) was used to deliver acoustic startle stimuli via headphones and record and score the corresponding electro myographic activity from the orbicularis oculi muscle. Two disposable electrodes (sensor area 12 mm2) were placed approximately 0.75-1cm below the pupil on the orbicularis oculi muscle and 3rd reference electrode on the mastoid bone. The skin area at the electrode site was cleaned with a cotton swab saturated with rubbing alcohol, then prepared by gently rubbing a small amount of EEG & ECG Skin Prepping Gel (Signa Gel- Parker Laboratories Inc., Fairfield, New jersey, USA), and cleaned again with a cotton swab.

The session (a total of 56 trials) is started with 3 min acclimatization period with a 60 dB background noise level that is delivered continuously throughout the test session. The session is comprised from two blocks. block1: comprised from randomly delivered six trials of single 40 msec 120 dB "pulse alone" startle stimuli in order to evaluate the startle response, ten "pre" stimuli (at 74, 78, 82, 86 or 92 dB), and thirty "pre pulse" trials that consisted of a single 120 dB pulse preceded (120 msec inter-stimulus-interval) by a 20 msec pre pulse of 14, 18, 22, 26 or 32 dB above background (i.e., 74, 78, 82, 86 or 92 dB). Block1 trials were delivered on average 20 sec inter-trial-interval ITI (15-25 sec, total 46 trials). Block2: comprised of the last ten trials of "pulse alone" startle, at fixed 2 sec ITI in order to evaluate a measure of habituation in response to repeated delivery of the startling stimuli. Finally, prepulse inhibition (PPI) was calculated as the percent of the habituated response as follows [100-(max response to "pre pulse" trial / max response to "pulse alone" trial X 100)]

GSR - Galvanic Skin Response Electrodermal activity will be measured by the differences of the skin conductivity. Two 5 mm electrodes will be placed on fingers 2 and 4 of the non-dominant hand. The electrodes will be connected to sensor and amplifying receiver with a 10Hz sampling rate.

Different portions of the skin can show differences in conductivity, due to sweat related to stress. Thus, measuring the skin conductivity of the non-dominant hand was shown to reduce this variability.

Hypothesis of the study: 1) DDs lessen the level of anxiety and attention impairment in children undergoing gastroscopies. 2) DDs improve the satisfaction of children and their parents during gastroscopies.

The aim of this study is: 1) To explore the influence of DDs on the satisfaction of children and their parents undergoing gastroscopy, utilizing questioners. 2) To explore the effects of DDs on anxiety and attention of children and their parents, undergoing gastroscopies by means of GSR, startle response and pre-pulse inhibition (PPI) tests and measuring anxiety-related biologic indices.

Patients and Methods: This randomized, controlled study will be conducted with children undergoing deep sedation during pediatric upper gastrointestinal endoscopies in the Gastroenterology institute of the Emek Medical Center,Afula, Israel. One hundred children (age 1-18 years) scheduled to undergo deep sedation and elective gastroscopy will be enrolled. During enrollment, the potential clown involvement will be explained to parents. Patients will be assigned to one of two groups: Group 1:children and their parents with the presence of DD upon arrival to the Gastroenterology institute and throughout the induction of sedation, gastroscopy and recovery. Group 2: children and their parents undergoing gastroscopy with deep sedation without the presence of a DD.

The randomization process: In Afula Medical Center, the investigators perform gastroscopies weekly. During the study period the investigators will perform the gastroscopies one week with the DD and one week without the DD.The patients will not be aware to that fact that in some weeks the DD is participating during the sedation induction in some of the patients (every other week). The DD will use various methods for entertaining the child and alleviate stress according to the child's age. The parents and the children will be given anxiety questioners to fill before the induction of sedation. At the end of the gastroscopy the parents and the children will be given satisfaction questioners. The children will perform Pre-Pulse inhibition (PPI) test and GSR before and after the gastroscopy to assess physiological and biological emotional and cognitive consequences. The parents will perform PPI test and GSR before, during and after the gastroscopy (no caffeine or nicotine consumption will be allowed 30min before examination). The anesthesiologist and the nurse at the recovery room will fill a questioner evaluating the behavior of the child during the induction of sedation and awakening. While inserting an IV line blood spots will be taken for stress hormones: cortisol, epinephrine, and norepinephrine. The following physical indices will be measured: blood pressure, pulse, saturation and body temperature. The amount of drugs given for deep sedation will be evaluated.

The current study hold two major innovativeness: (a) The effects of DD as part of the medical team in gastroscopy in children. (b) The physiological and biological evaluation of the emotional and cognitive consequences in children and their parents during gastroscopy.

Statistical analysis:

The study design is Mixed design (2X3), with DD as between subject factor (with or without DD) and stage of treatment as within subject factor (prior, during and after gastroscopy examination).Thus, we will conduct a Two-Way ANOVA (2X3) with post hoc Tukey's test. Significant interactions will be further analyzed with One-Way ANOVA. Moreover to relate physiological and biological measurement to questioner items, Pearson's correlations will be calculated.

The study schedule:

  1. Recruitment: 1.5 year
  2. Study period: for each patient the study will be held during the day of gastroscopy.
  3. Examination of blood serum by ELISA: 3 months.

3. Analysis of results: three months 4. Targeted date as to completion of project: two years from the study beginning.

Project staff:

  1. Dr Peleg Sarit - Board certified in Pediatrics and Pediatric Gastroenterology and Nutrition.
  2. Dr Rinawi Firas - Board certified in Pediatrics and Pediatric Gastroenterology and Nutrition.
  3. Dr Efrat Rachel - Board certified in Anesthesiology and Pediatrics.
  4. Professor Avital Avi - Behavioral Neuroscience Lab, Head.
  5. Mrs Lazimi Ilanit - Pediatric and Pediatric Gastroenterology nurse.
  6. Mr Yaron (Sancho) Goshen - Experienced DD.
  7. Mrs Yaara Tirosh Kamienchick - Research coordinator. Institutional overview: Dr Peleg Sarit, Pediatric Gastroenterology Unit, Emek Medical Center, Shderot Itzhak Rabin 21 Afula, 18101, Israel Phone: +972-4-6494104 Fax: +972-4-6495532 Email: Peleg_sa@clalit.org.il

Ethics:

The study will be conducted according to the ethical principles of the Declaration of Helsinki. Informed consent will be obtained following explicit description of the study outline and alternatives for participation. It will be made clear that declining to participate in the study will not jeopardize, in any way, the quality of care received. The signed consent will be filed in the patient's medical record. The principal investigators will have full access to the data prior to publication. CRFs will be identified and coded by study number and initials only.

Study Type

Interventional

Enrollment (Actual)

99

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Afula, Israel, 1834111
        • Emek Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 year to 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Children aged 1-18 years undergoing gastroscopy.
  • Informed consent of the parents

Exclusion Criteria:

  • Developmental delay or neurologic disease
  • Children who underwent endoscopy in the past
  • Parents that don't agree to participate in the study
  • ASA≥3
  • Children or parents hearing problem.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Children and their parents with the presence of Dream Doctors
The DD will use various methods for entertaining the child and alleviate stress . The parents and the children will be given anxiety and satisfaction questionnaires. The children and parents will perform Pre-Pulse inhibition (PPI) test and GSR. In addition, stress hormones will be assessed (cortisol, epinephrine, and norepinephrine) and the following physical indices will be measured: blood pressure, pulse, saturation and body temperature. The amount of drugs given for deep sedation will be evaluated.
children and their parents with and without the presence of DD upon arrival to the Gastroenterology institute and throughout the induction of sedation, gastroscopy and recovery.
Other Names:
  • dream doctor
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of PPI and GSR
Other Names:
  • PPI GSR
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of stress hormones.
Other Names:
  • stress hormones
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of blood pressure, pulse, saturation and body temperature.
Other Names:
  • physiological indices
Placebo Comparator: Children and their parents without the presence of DD
No DD during the gastroscopy. The parents and the children will be given anxiety and satisfaction questionnaires. The children and parents will perform Pre-Pulse inhibition (PPI) test and GSR. In addition, stress hormones will be assessed (cortisol, epinephrine, and norepinephrine) and the following physical indices will be measured: blood pressure, pulse, saturation and body temperature. The amount of drugs given for deep sedation will be evaluated.
children and their parents with and without the presence of DD upon arrival to the Gastroenterology institute and throughout the induction of sedation, gastroscopy and recovery.
Other Names:
  • dream doctor
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of PPI and GSR
Other Names:
  • PPI GSR
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of stress hormones.
Other Names:
  • stress hormones
evaluation of stress in children undergoing gastroscopy with sedation with and without the presence of a dream doctor by measurement of blood pressure, pulse, saturation and body temperature.
Other Names:
  • physiological indices

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Level of anxiety in children undergoing gastroscopies measured by biological indices (blood pressure)
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The following physical indices will be measured: blood pressure (mmHG)
Up to 12 hours during the day of gastroscopy for each patient.
Level of anxiety in children undergoing gastroscopies measured by biological indices (pulse)
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The following physical indices will be measured: pulse per minute
Up to 12 hours during the day of gastroscopy for each patient.
Level of anxiety in children undergoing gastroscopies measured by biological indices (saturation)
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The following physical indices will be measured: saturation meaning level of oxygen in blood with pulse oximeter in units
Up to 12 hours during the day of gastroscopy for each patient.
Level of anxiety in children undergoing gastroscopies measured by biological indices (body temperature)
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The following physical indices will be measured: body temperature in celsius degrees
Up to 12 hours during the day of gastroscopy for each patient.
Level of anxiety in children undergoing gastroscopies measured by biological indices (sedation drug level)
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The following physical indices will be measured:The amount of drugs given for deep sedation will be evaluated, in milligrams per kilogram body weight.
Up to 12 hours during the day of gastroscopy for each patient.
level of anxiety in children undergoing gastroscopies and their parents measured by PPI
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The investigators would use a monitoring device that would assess startle reflex reaction measured by blinking of the eye. Monitoring would be done with electrodes of EMG device that would be located on orbicularis oculi muscle and will monitor response. Startle reflex response (anxiety)- Assessed by millivolts registered by electromyography (EMG) electrodes.
Up to 12 hours during the day of gastroscopy for each patient.
level of anxiety in children undergoing gastroscopies and their parents measured by GSR
Time Frame: Up to 12 hours during the day of gastroscopy for each patient.
The investigators would use a monitoring device that would assess physiological reactivity by measurement of skin conductance (galvanic skin response).
Up to 12 hours during the day of gastroscopy for each patient.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 30, 2016

Primary Completion (Actual)

July 18, 2018

Study Completion (Actual)

July 18, 2018

Study Registration Dates

First Submitted

January 10, 2016

First Submitted That Met QC Criteria

January 28, 2016

First Posted (Estimate)

January 29, 2016

Study Record Updates

Last Update Posted (Actual)

October 3, 2018

Last Update Submitted That Met QC Criteria

October 2, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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