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Pediatric Integrative Medicine Trial Pilot (PIM)

Primary Purpose

Pain, Nausea, Vomiting

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
PIM consult and service provision
Usual care
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pain focused on measuring pain, nausea/vomiting, anxiety, complementary and alternative medicine, pediatric, oncology, cost-effectiveness

Eligibility Criteria

undefined - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • (i) all children, aged 0-16 years, who are admitted to Pediatric Oncology, General Pediatrics and Pediatric Cardiology at the Stollery Children's Hospital, Edmonton, Canada who
  • (ii) can communicate in English; and
  • (iii) give informed consent/assent

Exclusion Criteria:

  • (i) cannot communicate in English;
  • (ii) lack of parent availability to participate; or
  • iii) lack of informed consent.

Sites / Locations

  • Stollery Childrens' Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Usual care

PIM consult and service provision

Arm Description

Usual care provided to pediatric inpatients

Pediatric integrative medicine service (PIM) through which pediatric inpatients will have the option of supplementing their usual care with acupuncture/acupressure, massage, and/or reiki

Outcomes

Primary Outcome Measures

Enrollment
Enrollment of study participants over length of study which will inform conduct of a larger study in this population

Secondary Outcome Measures

Change in pain
For pre-verbal children: Faces, Legs, Activity, Cry, Consolability tool Verbal children: faces Pain Scale-Revised
Change in nausea/vomiting
Baxter Retching Faces scale
Change in anxiety
Pediatrics Anxiety Faces scale
Incidence of adverse events
BC Children's Hospital Patient Safety Questionnaire; Canadian Pediatric Trigger tool
Parent satisfaction with patient care
Hospital's standardized satisfaction survey; State-Trait Anxiety Invenvtory
Length of hospital stay

Full Information

First Posted
December 16, 2013
Last Updated
May 3, 2017
Sponsor
University of Alberta
Collaborators
Lotte & John Hecht Memorial Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02028832
Brief Title
Pediatric Integrative Medicine Trial Pilot
Acronym
PIM
Official Title
Pilot Study of Pediatric Integrative Medicine in Pediatric Oncology, General Pediatrics and Pediatric Cardiology
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alberta
Collaborators
Lotte & John Hecht Memorial Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will investigate if adding complementary therapies such as acupuncture, massage and reiki to inpatient pediatric care is feasible and what the effects are on outcomes such as patient symptoms, cost, safety, satisfaction and length of stay.
Detailed Description
Study Objective: To determine if a pediatric integrative medicine (PIM) service is effective in reducing overall symptoms of pain, nausea/vomiting, and/or anxiety (PNVA), length of stay, and costs, in hospitalized children when compared to conventional care. In this context, "integrative" refers to a combined approach of complementary and conventional medical therapies in an evidence-based fashion. Design: cluster trial; 2-arm controlled evaluation study in pediatric oncology, general pediatrics and pediatric cardiology. Intervention will be offered during a 6-month PIM period following a 6 month control period. Population: Inclusion criteria: (i) In-patients in participating division and (ii) informed consent/assent. Exclusion criteria: (i) lack of parent participation, fluency in English, or informed consent Intervention: Recommendations for specific CAM therapies will be determined by a staff PIM pediatrician. Any combination of the following CAM therapies (dose, duration, amount to be based on patient need as assessed by CAM provider, patient, and parent): acupuncture/acupressure, massage, Reiki; all are to be offered in addition to usual care. Control: Usual care. Outcomes: Primary outcome: feasibility (i.e enrollment); Secondary outcomes: (i) PNVA symptom management, (ii) need for conventional pharmacotherapy, (iii) adverse events; (iv) parent and health care provider satisfaction with care provided, v) length of stay; and vi) cost-effectiveness (analysis of this outcome to be limited to patients admitted for at least 2 days and for not more than 30 days). Significance: To our knowledge, this study will be the first comparative effectiveness trial to assess the impact of PIM for hospitalized children with cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Nausea, Vomiting, Anxiety
Keywords
pain, nausea/vomiting, anxiety, complementary and alternative medicine, pediatric, oncology, cost-effectiveness

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
872 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
Usual care provided to pediatric inpatients
Arm Title
PIM consult and service provision
Arm Type
Experimental
Arm Description
Pediatric integrative medicine service (PIM) through which pediatric inpatients will have the option of supplementing their usual care with acupuncture/acupressure, massage, and/or reiki
Intervention Type
Procedure
Intervention Name(s)
PIM consult and service provision
Intervention Description
If service is requested, treatment options include acupuncture/acupressure, massage, and reiki
Intervention Type
Procedure
Intervention Name(s)
Usual care
Intervention Description
Usual care consists of all conventional care options in pediatric oncology including medication and other therapies.
Primary Outcome Measure Information:
Title
Enrollment
Description
Enrollment of study participants over length of study which will inform conduct of a larger study in this population
Time Frame
up to 5 days
Secondary Outcome Measure Information:
Title
Change in pain
Description
For pre-verbal children: Faces, Legs, Activity, Cry, Consolability tool Verbal children: faces Pain Scale-Revised
Time Frame
up to 5 days
Title
Change in nausea/vomiting
Description
Baxter Retching Faces scale
Time Frame
up to 5 days
Title
Change in anxiety
Description
Pediatrics Anxiety Faces scale
Time Frame
up to 5 days
Title
Incidence of adverse events
Description
BC Children's Hospital Patient Safety Questionnaire; Canadian Pediatric Trigger tool
Time Frame
up to 5 days
Title
Parent satisfaction with patient care
Description
Hospital's standardized satisfaction survey; State-Trait Anxiety Invenvtory
Time Frame
up to 5 days
Title
Length of hospital stay
Time Frame
up to 5 days
Other Pre-specified Outcome Measures:
Title
Resource Utilization/Cost
Description
Resource utilization and related costs will be compared between study arms
Time Frame
Analysis of this outcome to be limited to patients admitted for at least 2 days and for not more than 30 days

10. Eligibility

Sex
All
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (i) all children, aged 0-16 years, who are admitted to Pediatric Oncology, General Pediatrics and Pediatric Cardiology at the Stollery Children's Hospital, Edmonton, Canada who (ii) can communicate in English; and (iii) give informed consent/assent Exclusion Criteria: (i) cannot communicate in English; (ii) lack of parent availability to participate; or iii) lack of informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sunita Vohra, MD, MSc
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stollery Childrens' Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Pediatric Integrative Medicine Trial Pilot

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