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Homeopathic Cold Remedy for Children Study

Primary Purpose

Upper Respiratory Tract Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Hyland's Cold 'n Cough 4 kids
placebo
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Upper Respiratory Tract Infections focused on measuring children, upper respiratory tract infections, homeopathy

Eligibility Criteria

2 Years - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • clinical diagnosis of upper respiratory tract infection
  • duration of symptoms < 7 days
  • Parent who speaks English

Exclusion Criteria:

  • history of asthma
  • on any prescribed medication
  • prescribed any medication other than acetaminophen or ibuprofen at index visit
  • use of homeopathic remedy within 48 hours of index visit

Sites / Locations

  • University of Washington Medical Center- Roosevelt Pediatric Care Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Homeopathic cold remedy

placebo

Arm Description

5 ml of homeopathic cold remedy given by mouth up to 6 times per day as needed for cold symptoms

5 ml of placebo given by mouth up to 6 times per day as needed for cold symptoms

Outcomes

Primary Outcome Measures

Change in Severity of Cold Symptoms
Parents measured change in runny nose, cough, nasal congestion and sneezing severity one hour after administering a dose of study medication up to the first 10 doses of study medication. Change in symptom rated from 0 to 6, with 0 indicative of the symptom being much worse and 6 indicative of the symptom being much improved. The unit of analysis for each outcome was doses of medication. Each participant could contribute data on 0 - 10 doses.

Secondary Outcome Measures

Change in Non-specific Symptoms
Parents measured change in severity of irritability, lethargy, fussiness, and appetite one hour after administering a dose of study medication up to the first 10 doses of study medication. Change in symptom rated from 0 to 6, with 0 indicative of the symptom being much worse and 6 indicative of the symptom being much improved. The unit of analysis for each outcome was doses of medication. Each participant could contribute data on 0 - 10 doses.
Functional Status
Change in functional status of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents rated 5 activities (vigorous activity, activities that require concentration, activities with family or friends, appetite and sleep) daily for 3 days in their child and again at the 7-10 day follow-up. Functional status scores range from 0 to 15, with higher scores indicative of better functional status.
Health Status
Change in health status of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents rated health status on 1-10 scale with 1 indicating perfect health and 10 indicating very sick. Health status rated on first 3 days of study and again at the 7-10 day follow-up
Overall Symptom Severity
Change in cold symptoms of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents assessed severity of runny nose, cough, sneeze and congestion in their child using a 0-3 scale for each symptom, 0=none to 3= severe. Cold score is sum of scores for each symptom. Parents assessed cold score twice daily on study days 1-3 and at the 7-10 day follow-up

Full Information

First Posted
December 8, 2010
Last Updated
December 31, 2014
Sponsor
University of Washington
Collaborators
Standard Homeopathic Company
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1. Study Identification

Unique Protocol Identification Number
NCT01257503
Brief Title
Homeopathic Cold Remedy for Children Study
Official Title
Randomized Controlled Trial of a Homeopathic Cold Remedy for Children
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Standard Homeopathic Company

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A randomized controlled trial of a commercially available homeopathic cold remedy will be conducted. A total of 400 children, 2-5 years old, diagnosed with an upper respiratory tract infection will be randomized to receive either the homeopathic remedy or placebo. Parents of study children will administer 5 ml of the study medication up to 6 times per day as needed to treat cold symptoms. One hour after giving a dose the parent will rate change in symptoms (for up to the first 10 doses). In addition, parents will rate their child's overall symptom severity and functional status over the first 3 days of the cold. It is postulated that children receiving the active homeopathic remedy will have better symptom relief and that their symptom severity and functional status will improve more rapidly than those receiving placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Upper Respiratory Tract Infections
Keywords
children, upper respiratory tract infections, homeopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
263 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Homeopathic cold remedy
Arm Type
Experimental
Arm Description
5 ml of homeopathic cold remedy given by mouth up to 6 times per day as needed for cold symptoms
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
5 ml of placebo given by mouth up to 6 times per day as needed for cold symptoms
Intervention Type
Drug
Intervention Name(s)
Hyland's Cold 'n Cough 4 kids
Intervention Description
5 ml PO q4h prn cold symptoms
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
liquid made to look like the active homeopathic remedy
Primary Outcome Measure Information:
Title
Change in Severity of Cold Symptoms
Description
Parents measured change in runny nose, cough, nasal congestion and sneezing severity one hour after administering a dose of study medication up to the first 10 doses of study medication. Change in symptom rated from 0 to 6, with 0 indicative of the symptom being much worse and 6 indicative of the symptom being much improved. The unit of analysis for each outcome was doses of medication. Each participant could contribute data on 0 - 10 doses.
Time Frame
Parents assessed change in symptom 1 hour after a dose of study medication
Secondary Outcome Measure Information:
Title
Change in Non-specific Symptoms
Description
Parents measured change in severity of irritability, lethargy, fussiness, and appetite one hour after administering a dose of study medication up to the first 10 doses of study medication. Change in symptom rated from 0 to 6, with 0 indicative of the symptom being much worse and 6 indicative of the symptom being much improved. The unit of analysis for each outcome was doses of medication. Each participant could contribute data on 0 - 10 doses.
Time Frame
Parents assessed change in symptom 1 hour after dose of study medication
Title
Functional Status
Description
Change in functional status of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents rated 5 activities (vigorous activity, activities that require concentration, activities with family or friends, appetite and sleep) daily for 3 days in their child and again at the 7-10 day follow-up. Functional status scores range from 0 to 15, with higher scores indicative of better functional status.
Time Frame
10 days
Title
Health Status
Description
Change in health status of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents rated health status on 1-10 scale with 1 indicating perfect health and 10 indicating very sick. Health status rated on first 3 days of study and again at the 7-10 day follow-up
Time Frame
10 days
Title
Overall Symptom Severity
Description
Change in cold symptoms of child during the 7-10 days after the index visit for an upper respiratory tract infection. Parents assessed severity of runny nose, cough, sneeze and congestion in their child using a 0-3 scale for each symptom, 0=none to 3= severe. Cold score is sum of scores for each symptom. Parents assessed cold score twice daily on study days 1-3 and at the 7-10 day follow-up
Time Frame
10 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: clinical diagnosis of upper respiratory tract infection duration of symptoms < 7 days Parent who speaks English Exclusion Criteria: history of asthma on any prescribed medication prescribed any medication other than acetaminophen or ibuprofen at index visit use of homeopathic remedy within 48 hours of index visit
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James A Taylor, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington Medical Center- Roosevelt Pediatric Care Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98105
Country
United States

12. IPD Sharing Statement

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Homeopathic Cold Remedy for Children Study

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