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CompletedNCT03435354PAToolKitUpdated Aug 29, 2023

Enhanced Physical Activity Support in Congenital Heart Disease Clinical Care

An interventional study of Physical activity counselling in Congenital Heart Disease, sponsored by Children's Hospital of Eastern Ontario. Completed at 3 sites in Canada. Open to participants aged 5 Years to 17 Years. Per ClinicalTrials.gov, last updated 2023-08-29.

Sponsored by Children's Hospital of Eastern Ontario · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
155
Allocation
Randomized
Ages
5 Years to 17 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 90 studies in Heart Defects, Congenital with a site in Canada — 16 open to participants now, 22 under way, 2 of them phase 3. Heart Defects, Congenital · Canada.

Enrollment
19th of 69
155 · median 63
Started
2018
with 6 others
No phase
47 of 90
8 open now
Registered
42nd of 90
by date
Lead sponsor
6 of 90
Children's Hospital of Eastern Ontario

Among the 90 studies in Heart Defects, Congenital with a site in Canada, this one is the 19th largest by enrollment of the 69 interventional ones that give a count, is one of 7 that started in 2018, is one of 47 with no phase, and was the 42nd registered.

Heart Defects, Congenital

991 studies on the registry are indexed under Heart Defects, Congenital; 251 are open to participants now.

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Open to participants now

16 of the 90 studies in Heart Defects, Congenital with a site in Canada are open now. Recruiting first, the newest first:

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A study can be open while its sites in Canada have not opened yet or have stopped. Only those recruiting at a site in Canada →

Who these studies take

Of the 154 Heart Defects, Congenital studies recruiting now, 67 (44%) set no upper age limit and 79 (51%) stop at 75 or younger; 110 take children under 18; 25 take healthy volunteers.

This study: 5 Years to 17 Years · all sexes · no healthy volunteers.

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02

Study 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).

Read the 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.

03

Conditions studied

  • Congenital Heart Disease

Keywords

  • Physical activity
  • Quality of life
  • Activity motivation
  • Children
  • Adolescents
  • Cluster-randomized trial
04

Who can participate

Ages eligible
5 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
155 participants (actual)

Study arms

  • Experimental
    Intervention

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

    Behavioral: Physical activity counselling

  • No intervention
    Usual Care

    Cardiac clinic visit with usual care but no physical activity counselling

Interventions

  • BehavioralPhysical activity counselling

    Clinician counselling about physical activity using standardized tools to promote daily physical activity.

    Also known as: PA counselling

06

What researchers measure

Primary outcomes

  1. Change in daily physical activity

    Pedometer step counts per day

    Time frame: Baseline then first week of each month for 6 months

Secondary outcomes

  1. 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).

    Time frame: Baseline, 6 months

  2. Change in quality of life

    Pediatric Quality of Life Inventory (PedsQL), score range 0 to 100, higher score is better quality of life

    Time frame: Baseline, 6 months

  3. Change in physical literacy

    PLAY Tools Run2 and screening question

    Time frame: Baseline, 6 months

Other outcomes

  1. Clinic visit time

    Time from arrival to departure of patient for clinic visit

    Time frame: Baseline

  2. Number of PA encounters

    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

  3. Delivery of PA counselling

    Proportion of intervention patients who receive enhanced physical activity counselling during clinic visit

    Time frame: Through study completion, on average 6 months

  4. Advanced PA counselling

    Proportion of intervention patients who are referred to kinesiologist for additional support

    Time frame: Through study completion, on average 6 months

07

Study locations

3 sites
  • Stollery Children's Hospital
    Edmonton, Alberta, Canada
  • London Health Sciences Centre
    London, Ontario, Canada
  • Children's Hospital of Eastern Ontario
    Ottawa, Ontario K1H 8L1, Canada
08

References and documents

Individual participant data

Plan to share: Yes — Study is funded by CIHR. Data is required to be shared upon completion of the project.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Mar 2018 to primary completion in May 2023, 62 months.

Of 205 non-industry interventional studies with no phase under Heart Defects, Congenital, half reached primary completion within 35 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 53. This study's 62 months is above that.

Counting every sponsor, half of 223 studies reached it within 34 months; a quarter within 17 and three quarters within 57.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 31, 2018
First posted
Feb 19, 2018
StartActual
Mar 5, 2018
Primary completionActual
May 31, 2023
CompletionActual
May 31, 2023
Last update
Aug 29, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 29, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03435354
Lead 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
Responsible party
Dr. Pat Longmuir (Scientist, Assistant Professor, Children's Hospital of Eastern Ontario) — Principal investigator
First posted
Feb 19, 2018
Start date
Mar 5, 2018
Primary completion
May 31, 2023
Completion
May 31, 2023
Last update
Aug 29, 2023

Study contacts

Patricia Longmuir, PhD
principal investigator · Scientist

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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