The Effect of Pre Surgery Dog Visits on Post Surgery Consumption of Pain Medication

NCT ID: NCT00452738

Last Updated: 2015-04-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2007-04-30

Study Completion Date

2008-02-29

Brief Summary

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The objective of this study is to examine the effects of pre surgery dog visits as compared to a costumed character or parents-only on the consumption of pain medication after surgery. It is hypothesized that pre surgery dog visits will reduce post surgical stress and anxiety.

Detailed Description

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Recent research has revealed that children who are highly anxious prior to surgery experienced more problems post surgery. These problems included reporting of more pain and requested more pain medication during hospitalization and home follow up. Consumption of pain medication may not be the optimal pain management program. In contrast, numerous human-animal interaction studies have shown that animals tend to have a calming effect on people, reduce stress, and lesson anxiety. Therefore, the primary objective of this study is to examine the effect of pre surgery dog visits as compared to a costumed character or parents-only on the consumption of pain medication after surgery.

Conditions

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Post Tonsillectomy Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Interventions

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Therapy dog

Intervention Type BEHAVIORAL

Costumed character

Intervention Type BEHAVIORAL

Parents-only

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Tonsillectomy and Adenoidectomy (T/A)
* 4-7 years old
* Prescribed codeine and/or analgesics for postoperative pain

Exclusion Criteria

* Participant must not be afraid of dogs, or allergic to animal dander
* Chronic medical conditions other than T/A
* Developmentally delayed
* On psychotropic medications
Minimum Eligible Age

4 Years

Maximum Eligible Age

7 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Oklahoma State University Center for Health Sciences

OTHER

Sponsor Role lead

Principal Investigators

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Sherril M Stone, PhD

Role: PRINCIPAL_INVESTIGATOR

Oklahoma State University Center for Health Sciences

Stan Sherman, DO

Role: PRINCIPAL_INVESTIGATOR

Oklahoma State University Center for Health Sciences

Chaunda Capers, BS

Role: PRINCIPAL_INVESTIGATOR

Oklahoma State University Center for Health Sciences

Locations

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Oklahoma State University Surgi-Center

Tulsa, Oklahoma, United States

Site Status

Countries

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United States

References

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Other Identifiers

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2006036

Identifier Type: -

Identifier Source: org_study_id

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