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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01601197
Other study ID # 27518
Secondary ID
Status Recruiting
Phase Phase 3
First received May 13, 2012
Last updated October 23, 2012
Start date May 2012
Est. completion date May 2013

Study information

Verified date October 2012
Source University of Toronto
Contact Anna Taddio, PhD
Phone 416-978-8822
Email anna.taddio@utoronto.ca
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

Immunization injections are a significant source of pain for infants. Tactile stimulation (rubbing/applying pressure) may be an effective and feasible pain-relieving intervention - it is cost neutral, and has been shown to be effective in children and adults undergoing injections. The aim of this study is to determine the added benefit of tactile stimulation when added to other proven analgesic interventions during routine infant immunization injections.


Description:

Immunization injections are a significant source of pain for infants. At present, effective and feasible pain-relieving interventions include sugar water, fast injection without aspiration, and holding infants during the procedure. These methods, however, do not eliminate pain in all infants. Additional interventions are therefore needed.

Tactile stimulation (rubbing/applying pressure) has been shown to reduce injection pain in children and adults, and may be a suitable intervention for infant injections. It is cost neutral, requires no preparation, and is easily incorporated into practice.

The aim of this study is to determine the effectiveness of tactile stimulation when added to other proven analgesic interventions on reducing pain during infant immunization injections.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date May 2013
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 1 Month to 12 Months
Eligibility Inclusion Criteria:

- infants 1-12 months of age receiving routine immunization injections in an outpatient pediatric clinic in Toronto

Exclusion Criteria:

- impaired neurological development

- history of seizure

- use of topical anesthetics

- use of sedatives or narcotics within 24 hours

- fever or illness that would prevent administration of vaccine

- prior participation in the trial

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Tactile stimulation
Immunizer will rub the ipsilateral limb before, during and after immunization injection(s)

Locations

Country Name City State
Canada Dr. Tommy Ho Pediatric Clinic Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Infant Pain as assessed by the Modified Behavioral Pain Scale assessed from videotaped procedure First 15 seconds after injection No
Secondary Parent rating of infant pain using the Numerical Rating Scale first minute after injection No
Secondary Immunizer rating of infant pain using the Numerical Rating Scale first minute after injection No
Secondary Infant crying time assessed from videotaped procedure duration of crying after injection No
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