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Supported Exercise Programme for Adults With Congenital Heart Disease (SEACHange)

Primary Purpose

Congenital Disorder, Heart Diseases

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Exercise Programme
Sponsored by
Golden Jubilee National Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Congenital Disorder focused on measuring Exercise, Physical Activity

Eligibility Criteria

16 Years - 75 Years (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Living in Scotland
  • Diagnosis of congenital heart disease
  • Walks less than 450 metres on a 6 minute walk test (Group 1)
  • Walks more than 450 metres on a 6 minute walk test (Group 2)

Exclusion Criteria:

  • No access to internet or telephone
  • Non English speaking (If the pilot study is successful, we anticipate that materials and programmes could be translated and accessible to non English speakers)
  • Vulnerable adults
  • Severe aortic stenosis or severe left ventricular outflow tract obstruction (LVOTO)
  • Eisenmenger Physiology (ongoing study recruitment with SPVU)
  • Currently prescribed Advanced Pulmonary Vasodilator therapy

Sites / Locations

  • Golden Jubilee National Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Other

Other

Other

Arm Label

Study Group One

Study Group Two

Study Group One - phase 2

Study Group Two - phase 2

Arm Description

Six Minute Walk Test distance <450metres. Exercise programme including inspiratory muscle trainer for 12 weeks. Contact weekly (via phone or email).

Six Minute Walk Test distance >450metres. Exercise programme including walking for 12 weeks. Contact every second week (via phone or email).

Six Minute Walk Test distance <450metres. Exercise programme including inspiratory muscle trainer for 12 weeks. Contact weekly (via phone or email).

Six Minute Walk Test distance >450metres. Exercise programme including walking for 12 weeks. Contact every second week (via phone or email).

Outcomes

Primary Outcome Measures

Attendance rate
Determine the feasibility of introducing a supported exercise programme in to clinical practice. This will be measured through attendance to the programme and interaction with the online resource.
Attrition rate
Determine the feasibility of introducing a supported exercise programme by assessing attrition rate throughout the study period.

Secondary Outcome Measures

Change in six minute walk test (6MWT)
Change in six minute walk test distance (metres) between 0 and 12 weeks. Offers a simple, readily available and cost effective method for objective evaluation of functional exercise capacity during daily activity.
Change in Sniff Nasal Inspiratory Pressure (SNIP)
Change in Sniff Nasal Inspiratory Pressure (SNIP) between 0 and 12 weeks (study group one). Measured in cmH2O and is used to measure inspiratory muscle strength.
Change in Grip Strength
Change in grip strength. This is measured in pounds (lbs) using a myometer. It is a recognized method of assessing overall nutritional status and health in subjects with medical conditions.
Is there an improvement in level of psychological distress
Change in level of depression (measured using PHQ- 9 questionnaire). It is a reliable and validated self report questionnaire used to help clinicians screen for depression disorder.
Is there an improvement in level of psychological distress
Change in level of anxiety (measured using GAD-7 questionnaire). The GAD -7 is a self report questionnaire used to identify probable cases of generalised anxiety disorder. Recognised as a valid and reliable screening tool
Body mass Index (BMI)
Change in body mass index (measured in kg/m2). Weight (kgs) and height (metres) will be combined to report BMI in kg/m2
Body weight
Change in body weight (measured in kg)
Is there an improvement in bicep strength
Change in bicep strength. This is measured in newtons (N) using a non invasive strain guage/myometer
Is there an improvement in quadricep strength
Change in quadricep strength. This is measured in newtons (N) using a non invasive strain guage/myometer

Full Information

First Posted
April 7, 2017
Last Updated
July 30, 2019
Sponsor
Golden Jubilee National Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03262168
Brief Title
Supported Exercise Programme for Adults With Congenital Heart Disease
Acronym
SEACHange
Official Title
Supported Exercise Programme for Adults With Congenital Heart Disease (SEA CHange)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
June 2, 2017 (Actual)
Primary Completion Date
December 21, 2018 (Actual)
Study Completion Date
December 21, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Golden Jubilee National Hospital

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
This study will evaluate if the introduction of a supported exercise programme can improve physical and psychological well-being for adults with congenital heart disease.
Detailed Description
Congenital heart disease (CHD) describes heart defects present from birth. The majority of affected patients will require lifelong care to not only manage their medical condition, but also to offer support and guidance on living with their specific heart condition. Exercise and physical activity is one such area where patients often require support and advice. Recommendations are in place for health care providers to promote physical activity for this patient population. However, many health care providers find it difficult to know what level of exercise is reasonable or how to escalate current exercise programmes. The benefits of regular exercise are well known and evidence suggests that even a modest increase in physical activity can reduce morbidity, improve psychological wellbeing and protect against cardiovascular disease. This pilot study will determine the feasibility of introducing a supported exercise programme to clinical practice. The investigators aim to assess if improvements can be made in both physical and psychological well-being for adults with CHD who are living in Scotland. After initial assessment and baseline measurements are obtained, participants will follow a twelve week individualised programme. The investigators will keep in regular contact with the participant throughout and arrange interval and final assessments. The baseline measurements will be repeated during the final assessment at 12 weeks. Investigators anticipate that the study will also help to establish a programme that will help to improve the way adults who were born with a heart condition can be supported with physical activity on a long term basis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Disorder, Heart Diseases
Keywords
Exercise, Physical Activity

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants compete a six minute walk test (6MWT). Those who achieve less than 450 metres will be assigned to study group one. Participants who achieve greater than 450 metres on 6MWT will be assigned to study group two.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Group One
Arm Type
Other
Arm Description
Six Minute Walk Test distance <450metres. Exercise programme including inspiratory muscle trainer for 12 weeks. Contact weekly (via phone or email).
Arm Title
Study Group Two
Arm Type
Other
Arm Description
Six Minute Walk Test distance >450metres. Exercise programme including walking for 12 weeks. Contact every second week (via phone or email).
Arm Title
Study Group One - phase 2
Arm Type
Other
Arm Description
Six Minute Walk Test distance <450metres. Exercise programme including inspiratory muscle trainer for 12 weeks. Contact weekly (via phone or email).
Arm Title
Study Group Two - phase 2
Arm Type
Other
Arm Description
Six Minute Walk Test distance >450metres. Exercise programme including walking for 12 weeks. Contact every second week (via phone or email).
Intervention Type
Other
Intervention Name(s)
Exercise Programme
Intervention Description
Complete background demographics, Sniff Nasal Inspiratory Pressure (study group one only), grip strength, muscle strength, PHQ-9 and GAD-7 questionnaires.
Primary Outcome Measure Information:
Title
Attendance rate
Description
Determine the feasibility of introducing a supported exercise programme in to clinical practice. This will be measured through attendance to the programme and interaction with the online resource.
Time Frame
12 weeks (for each phase)
Title
Attrition rate
Description
Determine the feasibility of introducing a supported exercise programme by assessing attrition rate throughout the study period.
Time Frame
12 weeks (for each phase)
Secondary Outcome Measure Information:
Title
Change in six minute walk test (6MWT)
Description
Change in six minute walk test distance (metres) between 0 and 12 weeks. Offers a simple, readily available and cost effective method for objective evaluation of functional exercise capacity during daily activity.
Time Frame
12 weeks (for each phase)
Title
Change in Sniff Nasal Inspiratory Pressure (SNIP)
Description
Change in Sniff Nasal Inspiratory Pressure (SNIP) between 0 and 12 weeks (study group one). Measured in cmH2O and is used to measure inspiratory muscle strength.
Time Frame
12 weeks (for each phase)
Title
Change in Grip Strength
Description
Change in grip strength. This is measured in pounds (lbs) using a myometer. It is a recognized method of assessing overall nutritional status and health in subjects with medical conditions.
Time Frame
12 weeks (for each phase)
Title
Is there an improvement in level of psychological distress
Description
Change in level of depression (measured using PHQ- 9 questionnaire). It is a reliable and validated self report questionnaire used to help clinicians screen for depression disorder.
Time Frame
12 weeks (for each phase)
Title
Is there an improvement in level of psychological distress
Description
Change in level of anxiety (measured using GAD-7 questionnaire). The GAD -7 is a self report questionnaire used to identify probable cases of generalised anxiety disorder. Recognised as a valid and reliable screening tool
Time Frame
12 weeks (for each phase)
Title
Body mass Index (BMI)
Description
Change in body mass index (measured in kg/m2). Weight (kgs) and height (metres) will be combined to report BMI in kg/m2
Time Frame
12 weeks (for each phase)
Title
Body weight
Description
Change in body weight (measured in kg)
Time Frame
12 weeks (for each phase)
Title
Is there an improvement in bicep strength
Description
Change in bicep strength. This is measured in newtons (N) using a non invasive strain guage/myometer
Time Frame
12 weeks (for each phase)
Title
Is there an improvement in quadricep strength
Description
Change in quadricep strength. This is measured in newtons (N) using a non invasive strain guage/myometer
Time Frame
12 weeks (for each phase)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Living in Scotland Diagnosis of congenital heart disease Walks less than 450 metres on a 6 minute walk test (Group 1) Walks more than 450 metres on a 6 minute walk test (Group 2) Exclusion Criteria: No access to internet or telephone Non English speaking (If the pilot study is successful, we anticipate that materials and programmes could be translated and accessible to non English speakers) Vulnerable adults Severe aortic stenosis or severe left ventricular outflow tract obstruction (LVOTO) Eisenmenger Physiology (ongoing study recruitment with SPVU) Currently prescribed Advanced Pulmonary Vasodilator therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maureen Mason, MSc
Organizational Affiliation
Golden Jubilee Research Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Golden Jubilee National Hospital
City
Clydebank
ZIP/Postal Code
G81 4DY
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plan to share individual data

Learn more about this trial

Supported Exercise Programme for Adults With Congenital Heart Disease

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