Comfort Talk for Pediatric Cardiac Catheterization

July 16, 2019 updated by: Jacqueline Viegas, The Hospital for Sick Children

The Impact of Comfort Talk on Anxiety Levels and Procedural Experience in a Pediatric Population Undergoing Cardiac Catheterization: A Prospective Randomized Controlled Trial

Background: Pre anaesthesia anxiety in children is a strong predictor of postoperative behavior challenges and outcomes. In addition, intra-operative stress can precipitate post-traumatic stress symptomatology. Comfort Talk, consisting of rapport, relaxation, and reframing of potentially stressful experiences, applied pre-operatively in script form, has been highly successful in alleviating anxiety and positively affecting procedural outcomes in adult patients undergoing interventional procedures. No published literature exists evaluating its' impact in paediatric cardiac catheterization. Purpose: To investigate the impact of comfort talk on the level of pre-induction anxiety, procedural and recovery experience, as well as short-term post-procedural behaviour and satisfaction after discharge in pediatric patients undergoing cardiac catheterization procedures. Design: Prospective randomized, double blind controlled trial. Participants: 160 children, ages 7-18 years, having a cardiac catheterization procedure under general anaesthesia. Intervention: Group A will be read a pre-procedure comfort talk script in the pre-procedure work-up area; Group B will be read a pre-extubation (before the breathing tube is removed) script ; Group C will be read a pre-procedure plus a pre-extubation script; Group D will not be read any script. All groups will be treated according to the standard of care approaches usually provided for anaesthesia, catheterization, and recovery. Outcomes: We will compare the effect of the script strategy on preoperative anxiety. Procedural and recovery measurements will include room time in the catheterization suite, time to discharge from the recovery room; drug use, vomiting, rebleeds, and cardiorespiratory stability. Postoperative behaviour will be assessed by questionnaire. Postoperative anxiety and pain will be secondary outcome measures using queries on 0-10 verbal self-report scales Hypotheses are:

  1. Patients being read a preoperative Comfort Talk script will experience less anxiety prior to anaesthesia induction.
  2. The reduction of anxiety prior to induction is associated with better immediate and short-term recovery outcomes.
  3. Patients being read a pre-extubation script will recover better than controls.
  4. The combination of a pre-procedure script and a pre-extubation script will have the greatest positive effect on physical and emotional well-being in the immediate recovery period and at short term follow-up.

Study Overview

Detailed Description

Among scheduled children for cardiac catheterization at the Labatt Family Health Center Cardiac Diagnostic and Interventional Unit (CDIU) , potential participants will be identified at their pre-catheterization clinic visit, the study explained, and informed consent obtained. On the day of their procedure, participants will be randomized to one of 4 groups. In the pre-catheterization work-up area, a modified Yale Preoperative Anxiety Scale (mYPAS) plus anxiety and pain self-ratings on verbal 0-10 scales will be obtained. In intervention groups A and C a pre-procedure Comfort Talk script will be read while the parent or guardian is present. Patients in Group B and D will not have a script read. The participants will be reassessed by mYPAS and asked to rate their level of pain and anxiety again on entering the procedure room and then care will continue as usual. The team members and anaesthesiologist will be blinded to the prior treatment and behave naturally but abstain from formalized use of hypnosis, invitation to imagery, use of scripts or electronic means of distraction. Induction of anaesthesia and the procedure will continue according to laboratory routine. Use of premedication will be permitted as per judgement of the anaesthesiologist. After induction a Paediatric Anesthesia Behaviour score (PAB) rating will be obtained. Prior to extubation, one of the CDIU nurses will read the pre-extubation script for those subjects in Groups B and C. Extubation and transfer to recovery will follow usual routine.

When the patients are transferred to the recovery room nurses will be unaware of group attribution. On waking from anaesthesia and up to 6 hours post-operatively, participants will again be asked to rate their levels of pain and anxiety at various intervals.

Within 24-48 hours of discharge from the hospital, families will be called to follow-up on their experience in the CDIU using the follow-up questionnaire regularly used by the CDIU nurses. At the same time the parents will be reminded to fill in the Post Hospitalization Behaviour Questionnaire (PHBQ) reflecting the child's behaviour in the first week after the procedure and mail it back in the stamped addressed envelope provided. If the envelope has not been mailed back within 10 days one of the research team members will call and complete it with the parents over the phone.

The pre-procedure script is based on a script that three large prospective randomized trials found to be effective in adults in reducing anxiety, pain, and complications of invasive image-guided procedures. It has been modified for use in paediatrics. The standardized script containing relaxing and hypnoidal language with suggestions for coping strategies will be read by CDIU RNs trained in Comfort Talk in the pre-catheterization work-up area. The pre-extubation script contains suggestions for healing, recovery, functioning of bodily systems, and acknowledgement of the patient's contribution.

Study Type

Interventional

Enrollment (Actual)

160

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

    • Ontario
      • Toronto, Ontario, Canada, M5G 1X8
        • Hospital for Sick Children

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

7 years to 18 years (ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Scheduled for cardiac catheterization
  • Procedure performed under general anesthetic
  • Ability to speak and understand English
  • No apparent cognitive impairments

Exclusion Criteria:

  • Active dissociative psychiatric disease

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
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Group A - Reading pre-procedure script
Patients will be read a pre-procedure comfort talk script in the pre-procedure work-up area
Patients will be read a pre-procedure comfort talk script in the pre-procedure work-up area
EXPERIMENTAL: Group B - Reading pre-extubation script
Patients will be read a pre-extubation script;
Patients will be read a comfort talk script before extubation
EXPERIMENTAL: Group C - Reading 2 scripts
Patients will be read a pre-procedure comfort talk script in the pre-procedure work-up area Patients will be read a pre-extubation script
Patients will be read a pre-procedure comfort talk script in the pre-procedure work-up area
Patients will be read a comfort talk script before extubation

Patients will be read a pre-procedure comfort talk script in the pre-procedure work-up area.

Patients will be read a comfort talk script before extubation

NO_INTERVENTION: Group D
Patients will not be read any script

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pre-anesthesia Anxiety
Time Frame: 3-15 min prior to anesthesia induction
Anxiety is measured by the modified Yale Preoperative Anxiety Scale (mYPAS) immediately upon entry into the operating room and introduction of the anesthesia mask to the child. The mYPAS consists of 22 items in five categories (activity, emotional expressivity, state of arousal, vocalization, and use of parents) and a maximal score of 100.
3-15 min prior to anesthesia induction
Postoperative Behavior
Time Frame: 1 week postoperatively
Measured with the Post Hospitalization Behaviour Questionnaire (PHBQ)
1 week postoperatively

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction with care
Time Frame: 24-48 hrs after discharge from the hospital
CDIU Post Cardiac Catherization follow-up phone survey addressing presence or absence of discomfort, bruising at the cath site, fever, return to normal bodily functions and activity, satisfaction with treatment from and communication with staff.
24-48 hrs after discharge from the hospital
Procedure Time
Time Frame: Duration of the cardiac catheterization procedure (1-4 hrs depending on complexity of case)
Duration of the cardiac catheterization procedure (1-4 hrs depending on complexity of case)
Duration of the cardiac catheterization procedure (1-4 hrs depending on complexity of case)
Recovery room time
Time Frame: within 24 hrs of procedure
Measure per recovery room log
within 24 hrs of procedure
Drug usage during procedure
Time Frame: 1-4 hrs
Amount of anesthesia drugs given in drug units
1-4 hrs
Drug usage during recovery
Time Frame: within 24 hrs
Amount of sedatives and narcotics in drug units
within 24 hrs
Antiemetics
Time Frame: within 28 hrs
Amount of antiememtics in drug units
within 28 hrs
Anesthesia induction behavior
Time Frame: within1 hr of anesthesia induction
Measured by the Pediatric Anesthesia Behaviour Score (PAB)
within1 hr of anesthesia induction
Nausea
Time Frame: within 28 hrs of procedure start
measured by frequency and severity
within 28 hrs of procedure start
Rebleeds
Time Frame: within 1 week of procedure
counts and severy
within 1 week of procedure
any pain
Time Frame: within 28 hrs of arrival
0-10 self-reporting scale
within 28 hrs of arrival
Self-reported anxiety
Time Frame: within 28 hrs of arrival
0-10 self-reporting scale
within 28 hrs of arrival

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jacquie Viegas, RN, Hospital for Sick Childen, Toronto, CA

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.

General Publications

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

January 1, 2015

Primary Completion (ACTUAL)

June 1, 2018

Study Completion (ACTUAL)

September 1, 2018

Study Registration Dates

First Submitted

January 21, 2015

First Submitted That Met QC Criteria

January 21, 2015

First Posted (ESTIMATE)

January 27, 2015

Study Record Updates

Last Update Posted (ACTUAL)

July 18, 2019

Last Update Submitted That Met QC Criteria

July 16, 2019

Last Verified

July 1, 2019

More Information

Terms related to this study

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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