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Enhanced Physical Activity Support in Congenital Heart Disease Clinical Care (PAToolKit)

Primary Purpose

Congenital Heart Disease

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Physical activity counselling
Sponsored by
Children's Hospital of Eastern Ontario
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Congenital Heart Disease focused on measuring Physical activity, Quality of life, Activity motivation, Children, Adolescents, Cluster-randomized trial

Eligibility Criteria

5 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients 5 to 17 years with CHD diagnoses classified as moderate or severe in complexity by the American College of Cardiology / American Heart Association joint guidelines.

Exclusion Criteria:

  • Cardiac intervention (catheterization or surgery) in preceding 6 months. Syndrome/diagnosis affecting physical activity (e.g., developmental disability) or the ability to complete the assessment questionnaires.

Sites / Locations

  • Stollery Children's Hospital
  • London Health Sciences Centre
  • Children's Hospital of Eastern Ontario

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Usual Care

Arm Description

Physical activity counselling during cardiac clinic visit with additional supports for community physical activity and access to a kinesiologist.

Cardiac clinic visit with usual care but no physical activity counselling

Outcomes

Primary Outcome Measures

Change in daily physical activity
Pedometer step counts per day

Secondary Outcome Measures

Change in physical activity adequacy and predilection
Children's Self-Perceived Adequacy and Predilection for Physical Activity Scale (total score, range 20 to 80 points, higher values are a better outcome).
Change in quality of life
Pediatric Quality of Life Inventory (PedsQL), score range 0 to 100, higher score is better quality of life
Change in physical literacy
PLAY Tools Run2 and screening question

Full Information

First Posted
January 31, 2018
Last Updated
August 28, 2023
Sponsor
Children's Hospital of Eastern Ontario
Collaborators
Stollery Children's Hospital, London Health Sciences Centre, CHEO Family Forum, Canadian Congenital Heart Alliance, Ontario Child Health Support Unit
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1. Study Identification

Unique Protocol Identification Number
NCT03435354
Brief Title
Enhanced Physical Activity Support in Congenital Heart Disease Clinical Care
Acronym
PAToolKit
Official Title
Impacting Child Physical and Mental Health Outcomes in Congenital Heart Disease: A Randomized, Controlled Trial of Enhanced Physical Activity Support in Clinical Care
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 5, 2018 (Actual)
Primary Completion Date
May 31, 2023 (Actual)
Study Completion Date
May 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Eastern Ontario
Collaborators
Stollery Children's Hospital, London Health Sciences Centre, CHEO Family Forum, Canadian Congenital Heart Alliance, Ontario Child Health Support Unit

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Our cluster randomized controlled trial of a novel clinical practice change will IMPACT the physical activity (PA) of children living with congenital heart defects (CHD) through our Innovative and pragmatic approach to systematically incorporate PA counselling within each clinic visit. Long-term, the focus is to prevent or treat the most common secondary morbidities of these patients (atherosclerosis, anxiety, depression) through enhanced PA. We have previously shown that home-based, PA interventions can increase daily PA and enhance PA motivation, motor skill and fitness when delivered via an intensive research intervention. Our objectives for this study are to Measure the feasibility and efficacy of PA counselling using clinical resources among paediatric CHD patients (daily PA, PA motivation, competence, quality of life) and on clinic systems (% patients counselled, clinic/kinesiology personnel support required, clinic visit time, # of PA questions). Our Patient-empowering, ready-to-use, self-explanatory "tool kit" of clinician PA resources and patient/family/clinician friendly searchable electronic PA database will be used to promote the Active lifestyles that are critically important to physical/mental health, peer socialization & childhood growth/development. 90% of children are not active enough for optimal health. We initially target children with CHD because they are less active than peers, and their most important secondary morbidities can be prevented or treated through PA. Our Collaborative approach with patients, their families and leaders in paediatric cardiac healthcare will optimize our "PA tool kit" and novel practice change for Translation to all paediatric CHD healthcare systems (primary, secondary, tertiary) through our pan-Canadian Cardiac Kids Quality of LIFFE Research and Knowledge Exchange Network, a collaborative of 10 patient/family support networks and 10 paediatric cardiac clinics in 6 provinces focused on Learning, Independence, Friends, Fitness & Emotional health (LIFFE).
Detailed Description
Inactive lifestyles have a huge cost to Canadians' health, our economy and healthcare system (3.7% of total healthcare costs, 2009=$6.8B19). If 10% of Canadians were more active, 25-yr healthcare costs would drop by $2.6B, $7.5B would be added to our economy, & 550,000 fewer Canadians would live with chronic disease. Congenital heart disease (CHD) is the most common congenital condition (12/1000 births) and a major health burden. 90% of CHD children live 4 to 8 decades with a 3-5X higher risk for atherosclerosis, anxiety or depression. Physical activity is known to decrease these important health risks. <10% of Canadian children are active enough for optimal health and, regardless of severity, CHD children are even less active. Individualized kinesiology support can improve physical activity (PA) skill, confidence and participation among CHD children but exceeds current clinical care resources. In response, our team of patients, parents, and clinicians developed a "tool kit" of 12 child/family-friendly PA resources to enable clinicians to better address the most important PA issues for these patients. Our randomized, controlled trial will evaluate a clinical practice change (systematic PA counselling with the PA tool kit plus PA in CHD database) on patient PA and health system outcomes in small (London), medium (Ottawa) and large (Edmonton) paediatric cardiac clinics. Randomization will be by week within each study site to prevent potential intervention cross contamination between children in clinic at the same time. Primary outcome is daily pedometer steps over 1 week. Secondary outcomes are quality of life (PedsQL), physical literacy (CAPL screen) and PA motivation (CSAPPA). Health system outcomes will be: % patients receiving intervention, clinic visit time, # of non-clinic contacts about PA, and need for kinesiology referral. Patient outcomes will be assessed during the CHD clinic visit and at 6 months, with pedometer steps also measured each month. We will enroll consecutive CHD patients with moderate or severe CHD, 5 - 17 yrs, & no other diagnosis affecting PA. Based on our data from previous PA studies among CHD patients and anticipating 10 patients/month, we would require 15 months of data collection (10% dropout) to obtain the 136 complete data sets required to provide 80% power to detect a clinically meaningful increase in daily PA of 1000 steps/day. Repeated measures ANOVA will evaluate study group impact (control/intervention) on pedometer steps. Secondary ANCOVA models will adjust for age, sex, treatment history and clinic site (Ottawa, London, Edmonton). Our research team combines expertise in clinical intervention trials (Longmuir) and study design and analyses (Willan) with patient (Graham) & family (Rouble) experience plus > 60 years of clinical expertise (Lougheed, Norozi, Mackie). All investigators have previous experience leading multi-site research projects and supervising graduate students. Graham (Can. Congenital Heart Alliance) will ensure intervention relevance and scalability to all Canadian CHD patients. CHEO Family Forum (Rouble) will provide parent input. Through this study, we will advance knowledge of healthy, active lifestyles & PA support for CHD patients & the health system impacts of current practice recommendations to promote PA to CHD patients at every clinical encounter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease
Keywords
Physical activity, Quality of life, Activity motivation, Children, Adolescents, Cluster-randomized trial

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster-randomized trial, with randomization by within each site by week (i.e., site-week)
Masking
Outcomes Assessor
Masking Description
Those conducting the post-intervention assessments will be blind to study group allocation.
Allocation
Randomized
Enrollment
155 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Physical activity counselling during cardiac clinic visit with additional supports for community physical activity and access to a kinesiologist.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Cardiac clinic visit with usual care but no physical activity counselling
Intervention Type
Behavioral
Intervention Name(s)
Physical activity counselling
Other Intervention Name(s)
PA counselling
Intervention Description
Clinician counselling about physical activity using standardized tools to promote daily physical activity.
Primary Outcome Measure Information:
Title
Change in daily physical activity
Description
Pedometer step counts per day
Time Frame
Baseline then first week of each month for 6 months
Secondary Outcome Measure Information:
Title
Change in physical activity adequacy and predilection
Description
Children's Self-Perceived Adequacy and Predilection for Physical Activity Scale (total score, range 20 to 80 points, higher values are a better outcome).
Time Frame
Baseline, 6 months
Title
Change in quality of life
Description
Pediatric Quality of Life Inventory (PedsQL), score range 0 to 100, higher score is better quality of life
Time Frame
Baseline, 6 months
Title
Change in physical literacy
Description
PLAY Tools Run2 and screening question
Time Frame
Baseline, 6 months
Other Pre-specified Outcome Measures:
Title
Clinic visit time
Description
Time from arrival to departure of patient for clinic visit
Time Frame
Baseline
Title
Number of PA encounters
Description
Number of times that patients contact the clinic between clinics for reasons related to physical activity
Time Frame
Through study completion on average 6 months
Title
Delivery of PA counselling
Description
Proportion of intervention patients who receive enhanced physical activity counselling during clinic visit
Time Frame
Through study completion, on average 6 months
Title
Advanced PA counselling
Description
Proportion of intervention patients who are referred to kinesiologist for additional support
Time Frame
Through study completion, on average 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients 5 to 17 years with CHD diagnoses classified as moderate or severe in complexity by the American College of Cardiology / American Heart Association joint guidelines. Exclusion Criteria: Cardiac intervention (catheterization or surgery) in preceding 6 months. Syndrome/diagnosis affecting physical activity (e.g., developmental disability) or the ability to complete the assessment questionnaires.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patricia Longmuir, PhD
Organizational Affiliation
Scientist
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stollery Children's Hospital
City
Edmonton
State/Province
Alberta
Country
Canada
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
Country
Canada
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Study is funded by CIHR. Data is required to be shared upon completion of the project.

Learn more about this trial

Enhanced Physical Activity Support in Congenital Heart Disease Clinical Care

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