Pediatric Preoperative Anxiety Clinical Trial
Official title:
Use of Handheld Audiovisual Devices to Treat Pediatric Preoperative Anxiety: A Randomized Control Trial.
| NCT number | NCT02286674 |
| Other study ID # | 201400076 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | November 2014 |
| Est. completion date | January 2017 |
| Verified date | August 2022 |
| Source | McLaren Health Care |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Anxiety in children undergoing surgery is a central concern to both parents and healthcare workers, including nurses, surgeons, and anesthesiologists. It has been ranked by anesthesiologists as one of the top five important low-morbidity anesthesia outcomes (1). This study would determine whether such devices would decrease anxiety in children prior to induction of anesthesia for outpatient surgery. Two hundred children ages 2-12 will be enrolled.
| Status | Completed |
| Enrollment | 200 |
| Est. completion date | January 2017 |
| Est. primary completion date | November 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 2 Years to 12 Years |
| Eligibility | Inclusion Criteria: 1. Ages 2-12 2. Outpatient surgery procedures 3. ASA I of II (No or mild systemic disease) 4. Parental/guardian ability to understand and willingness to sign written informed consent 5. Patient assent to use tablet, if they are randomized to the study group 6. Anesthetic plan includes sevoflurane inhalation induction as determined by the anesthesiologist Exclusion Criteria: 1. Psychoactive medications (e.g. antipsychotics, mood stabilizers, anxiolytics, antidepressants, narcotics) 2. Diagnosed psychiatric disease 3. Developmental disabilities 4. History of photosensitive seizures 5. Patient requiring sedative or narcotic medications prior to induction of anesthesia, as determined by the anesthesiologist. 6. Parental/guardian inability to understand or refusal to sign written informed consent 7. Patient unwillingness or inability to use tablet 8. Anesthetic plan does not include sevoflurane induction, as determined by anesthesiologist. 9. Non English speaking patient and/or parent/guardian |
| Country | Name | City | State |
|---|---|---|---|
| United States | McLaren Greater Lansing Hospital | Lansing | Michigan |
| Lead Sponsor | Collaborator |
|---|---|
| McLaren Health Care |
United States,
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* Note: There are 18 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Yale Preoperative Anxiety Score | Anytime prior to patient being ifnormed of group assignment | Baseline | |
| Primary | Yale Preoperative Anxiety Score | Approx 15-20 minutes after the study group participants receive a tablet | Upon patient spearation from parents Approx 15-20 minutes | |
| Primary | Yale Preoperative Anxiety Score | 1-32 minutes after #2 | Patient enters operating room 1-32 minutes | |
| Primary | Yale Preoperative Aniety Score | 1-2 minutes after #3 | Placement of face mask on patient ofr anesthetic delivery 1-2 minutes |