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Self-care in Older Frail Persons With Heart Failure Intervention (SOPHI)

Primary Purpose

Self Care, Heart Failure, Frailty

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Self-care in Older frail Persons with Heart failure Intervention (SOPHI)
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Self Care focused on measuring self care, heart failure, symptom management, exercise, nutrition

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients at geriatric clinic
  • Diagnosed with heart failure (independent of Ejection Fraction (EF): both patients with preserved EF or reduced EF can be included
  • New York Heart Association functional class II - III
  • Clinical frailty level 4-6 (moderate frailty)
  • Discharge from hospital to home

Exclusion Criteria:

  • New York Heart Associacion functional class I or IV
  • Clinical frailty level 1-3 (no/mild frailty) and 7-9 (severe frailty)
  • The patient is unable to perform gait tests due to visual (see a TV screen at a 3 meter distance), cognitive (assessed by nurse or doctor) or motor impairment (the patient should be able to stand up from sitting and have the ability to walk with or without a walker or other walking aid).
  • The patient is unable to follow instructions (assessed by nurse or doctor)

Sites / Locations

  • Karolinska Universitetssjukhuset, Tema Inflammation och Åldrande

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Self Care group

Control group

Arm Description

Patients who are randomized to the intervention Self Care group will get advice and support on physical excercise, nutrition and symptom management to perform at home for 12 weeks. Once a week, patients will come to the hospital for follow-up and to exercise with a physiotherapist.

Patients who are randomized to the Control group will receive ordinary health care (from an outpatient clinic), but will also be encouraged to follow recommendation of 150 minutes/week of moderate physical activity (12 weeks). To compensate for the extra attention received by the intervention group by the advice/support, the patients in the control group will be dialed with a nurse at 3, 6 and 9 weeks to discuss their current activity.

Outcomes

Primary Outcome Measures

Change in physical performance
The "Short Physical Performance Battery" is composed of "standing balance", "gait speed", and "timed repeated chair rise". The total score range from minimum 0 to maximum 12, with higher scores indicating better physical performance.

Secondary Outcome Measures

Symptom burden
Assessed by the questionnaire titled "The Memorial Symptom Assessment Scale- Heart Failure", that evaluates symptoms experienced by the patient in the last week (a total of 36 symptoms, for example pain, nausea, tiredness). A score of 0 is given to a symptom if it is absent. If the symptom is present, it is rated using a four-point rating scale (1-4) for frequency and severity, and a five-point rating scale (0-4) for distress of the symptom with higher scores indicating greater frequency, more severity and higher distress. For each symptom, the average of the frequency, severity and distress will be calculated to produce the outcome symptom burden (total scores ranging from minimum 0 to maximum 4, with higher scores indicating greater symptom burden).
Health related quality of life
Assessed with the Euroqol questionnaire titled "The EQ-5D". It comprises five questions about mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Answer options are no problems (score 1), moderate problems (score 2), severe/extreme problems (score 3). The results are converted into a single index value (minimum value 0 to maximum value 1). Higher value indicate better health related quality of life
Aerobic capacity/endurance
Assessed with the 6-minute walk test, the distance in meters covered over a time of 6 minutes
Frailty
Assessed by the scale titled "Clinical Frailty Scale". From the minimum value 1 (patient is very fit) to the maximum value 9 (terminally ill). Higher score indicates more frailty
Perceived physical effort
Assessed with the scale titled "Borg Category Ratio-10 Scale" of perceived exertion. The minimum value is 0 (nothing at all) to the maximum value 10 (extremely strong or maximal). Higher value indicate worse physical effort
Hand strength
Assessed with the hand-gripdynamometer (JAMAR)
Hospital readmissions
The number of hospital readmissions during a 12 month period will be retrieved from the patients medical record
Lower body strength
Sit to stand test measure the number of uprising from a chair during 30 seconds
Nutrition status
Assessed by the "Mini Nutritional Assessment" screening. The total score range from minimum 0 to maximum 14. Higher scores indicate better nutrition status
Inflammation marker
Plasma C-reactive protein (mg/L), reference interval value below 3 mg/L. Higher value indicate inflammation in the body
Sarcopenia
Measured by the criteria of European Working Group on Sarcopenia in Older People's

Full Information

First Posted
August 4, 2021
Last Updated
March 29, 2022
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05009706
Brief Title
Self-care in Older Frail Persons With Heart Failure Intervention
Acronym
SOPHI
Official Title
Self-care in Older Frail Persons With Heart Failure Intervention (SOPHI). Individualized Physical Exercise, Diet and Symptom Management- A Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
September 6, 2021 (Actual)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital

4. Oversight

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

5. Study Description

Brief Summary
The overall purpose of the randomized controlled study is to evaluate the effects of physical exercise, nutrition and symptom management on physical capacity in older, frail persons with heart failure.
Detailed Description
The randomized controlled study will be conducted in order to evaluate the effects of individual needs of physical exercise, nutrition, and symptom management in patients with heart failure who are frail and older. Patients discharged from a geriatric hospital will be recruited and included after informed consent. Two weeks after hospital discharge patients are randomized to intervention or control group. The intervention period is 3 months. With support from a physioterapeut, dietician and a registered nurse, the intervention will be performed in the participants´ home. Once a week participants will come to the hospital for physical exercise led by a physiotherapist. Once a week or every other week participants will meet a dietician and a nurse. Data will be collected at baseline, and 3 and 6 months after baseline. Data consist of e.g. study flow description, number of eligible patients, number of drop-outs, patients sociodemographic- and clinical data, physical function and performance, nutritional status, symptom burden, self-care, appetite, thirst, health-related quality of life. At 12 months after baseline, data will be collected on hospital admissions, reasons for hospital admissions, length of stay and mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Self Care, Heart Failure, Frailty
Keywords
self care, heart failure, symptom management, exercise, nutrition

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
212 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Self Care group
Arm Type
Experimental
Arm Description
Patients who are randomized to the intervention Self Care group will get advice and support on physical excercise, nutrition and symptom management to perform at home for 12 weeks. Once a week, patients will come to the hospital for follow-up and to exercise with a physiotherapist.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients who are randomized to the Control group will receive ordinary health care (from an outpatient clinic), but will also be encouraged to follow recommendation of 150 minutes/week of moderate physical activity (12 weeks). To compensate for the extra attention received by the intervention group by the advice/support, the patients in the control group will be dialed with a nurse at 3, 6 and 9 weeks to discuss their current activity.
Intervention Type
Other
Intervention Name(s)
Self-care in Older frail Persons with Heart failure Intervention (SOPHI)
Intervention Description
Patients who are randomized to the Self Care group will receive oral and written information, advice and support on following activities: excercise (from physiotherapist), nutrition (dietician) and symptom management (nurse), based on patient´s individual needs and abilities. The Self Care group will perform the activities daily at home. Once a week, patients come to the hospital to exercise with the support of a physiotherapist. Once a week or every other week patients will meet (at hospital or by phone) the dietician and nurse to solve possible problems and to follow-up food/nutrition intake and symptoms/symptom management.
Primary Outcome Measure Information:
Title
Change in physical performance
Description
The "Short Physical Performance Battery" is composed of "standing balance", "gait speed", and "timed repeated chair rise". The total score range from minimum 0 to maximum 12, with higher scores indicating better physical performance.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Symptom burden
Description
Assessed by the questionnaire titled "The Memorial Symptom Assessment Scale- Heart Failure", that evaluates symptoms experienced by the patient in the last week (a total of 36 symptoms, for example pain, nausea, tiredness). A score of 0 is given to a symptom if it is absent. If the symptom is present, it is rated using a four-point rating scale (1-4) for frequency and severity, and a five-point rating scale (0-4) for distress of the symptom with higher scores indicating greater frequency, more severity and higher distress. For each symptom, the average of the frequency, severity and distress will be calculated to produce the outcome symptom burden (total scores ranging from minimum 0 to maximum 4, with higher scores indicating greater symptom burden).
Time Frame
Baseline, 3 and 6 months
Title
Health related quality of life
Description
Assessed with the Euroqol questionnaire titled "The EQ-5D". It comprises five questions about mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Answer options are no problems (score 1), moderate problems (score 2), severe/extreme problems (score 3). The results are converted into a single index value (minimum value 0 to maximum value 1). Higher value indicate better health related quality of life
Time Frame
Baseline, 3 and 6 months
Title
Aerobic capacity/endurance
Description
Assessed with the 6-minute walk test, the distance in meters covered over a time of 6 minutes
Time Frame
Baseline, 3 and 6 months
Title
Frailty
Description
Assessed by the scale titled "Clinical Frailty Scale". From the minimum value 1 (patient is very fit) to the maximum value 9 (terminally ill). Higher score indicates more frailty
Time Frame
Baseline, 3 and 6 months
Title
Perceived physical effort
Description
Assessed with the scale titled "Borg Category Ratio-10 Scale" of perceived exertion. The minimum value is 0 (nothing at all) to the maximum value 10 (extremely strong or maximal). Higher value indicate worse physical effort
Time Frame
Baseline, 3 and 6 months
Title
Hand strength
Description
Assessed with the hand-gripdynamometer (JAMAR)
Time Frame
Baseline, 3 and 6 months
Title
Hospital readmissions
Description
The number of hospital readmissions during a 12 month period will be retrieved from the patients medical record
Time Frame
12 months
Title
Lower body strength
Description
Sit to stand test measure the number of uprising from a chair during 30 seconds
Time Frame
Baseline, 3 and 6 months
Title
Nutrition status
Description
Assessed by the "Mini Nutritional Assessment" screening. The total score range from minimum 0 to maximum 14. Higher scores indicate better nutrition status
Time Frame
Baseline, 3 and 6 months
Title
Inflammation marker
Description
Plasma C-reactive protein (mg/L), reference interval value below 3 mg/L. Higher value indicate inflammation in the body
Time Frame
Baseline, 3 and 6 months
Title
Sarcopenia
Description
Measured by the criteria of European Working Group on Sarcopenia in Older People's
Time Frame
Baseline, 3 and 6 months
Other Pre-specified Outcome Measures:
Title
Objective physical activity
Description
Measured with a non-invasive miniature electronic logger during 4-5 days per time frame
Time Frame
Baseline, 3 and 6 months
Title
Subjective physical activity
Description
Assessed by the instrument titled "International Physical Activity Questionnaire" (IPAQ). Measure the minutes of physical activity during a day.
Time Frame
Baseline, 3 and 6 months
Title
Experiences of patients
Description
A qualitative interview will be used to collect data on patient´s experiences of the intervention
Time Frame
3 months
Title
Self-care
Description
Assessed with the questionnaire titled "Self-care of chronic illness inventory" (30 questions). Minimum score is 28 and maximum score is 150. Higher score indicate better self care
Time Frame
Baseline, 3 and 6 months
Title
Appetite
Description
Assessed with the questionnaire titled "The Council on Nutrition Appetite Questionnaire" (8 questions)Failure". Minimum score is 8 and maximum score is 40. Higher score indicate better appetite
Time Frame
Baseline, 3 and 6 months
Title
Thirst distress
Description
Assessed with the questionnaire titled "Thirst Distress Scale for patients with Heart Failure" (8 questions) Minimum score is 8 and maximum score is 40. Higher score indicate higher thirst distress
Time Frame
Baseline, 3 and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients at geriatric clinic Diagnosed with heart failure (independent of Ejection Fraction (EF): both patients with preserved EF or reduced EF can be included New York Heart Association functional class II - III Clinical frailty level 4-6 (moderate frailty) Discharge from hospital to home Exclusion Criteria: New York Heart Associacion functional class I or IV Clinical frailty level 1-3 (no/mild frailty) and 7-9 (severe frailty) The patient is unable to perform gait tests due to visual (see a TV screen at a 3 meter distance), cognitive (assessed by nurse or doctor) or motor impairment (the patient should be able to stand up from sitting and have the ability to walk with or without a walker or other walking aid). The patient is unable to follow instructions (assessed by nurse or doctor)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nana Waldréus, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Universitetssjukhuset, Tema Inflammation och Åldrande
City
Huddinge
ZIP/Postal Code
14186
Country
Sweden

12. IPD Sharing Statement

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Self-care in Older Frail Persons With Heart Failure Intervention

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