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Self-care in Older Frail Persons With Heart Failure Intervention

Self-care in Older Frail Persons With Heart Failure Intervention (SOPHI). Individualized Physical Exercise, Diet and Symptom Management- A Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05009706
Acronym
SOPHI
Enrollment
212
Registered
2021-08-17
Start date
2021-09-06
Completion date
2025-03-31
Last updated
2022-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty, Heart Failure, Self Care

Keywords

self care, heart failure, symptom management, exercise, nutrition

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.

Interventions

OTHERSelf-care in Older frail Persons with Heart failure Intervention (SOPHI)

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.

Sponsors

Karolinska University Hospital
CollaboratorOTHER
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Change in physical performance3 monthsThe 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

MeasureTime frameDescription
FrailtyBaseline, 3 and 6 monthsAssessed 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
Hand strengthBaseline, 3 and 6 monthsAssessed with the hand-gripdynamometer (JAMAR)
Hospital readmissions12 monthsThe number of hospital readmissions during a 12 month period will be retrieved from the patients medical record
Lower body strengthBaseline, 3 and 6 monthsSit to stand test measure the number of uprising from a chair during 30 seconds
Nutrition statusBaseline, 3 and 6 monthsAssessed by the Mini Nutritional Assessment screening. The total score range from minimum 0 to maximum 14. Higher scores indicate better nutrition status
Inflammation markerBaseline, 3 and 6 monthsPlasma C-reactive protein (mg/L), reference interval value below 3 mg/L. Higher value indicate inflammation in the body
SarcopeniaBaseline, 3 and 6 monthsMeasured by the criteria of European Working Group on Sarcopenia in Older People's
Symptom burdenBaseline, 3 and 6 monthsAssessed 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 lifeBaseline, 3 and 6 monthsAssessed 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/enduranceBaseline, 3 and 6 monthsAssessed with the 6-minute walk test, the distance in meters covered over a time of 6 minutes
Perceived physical effortBaseline, 3 and 6 monthsAssessed 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

Other

MeasureTime frameDescription
Experiences of patients3 monthsA qualitative interview will be used to collect data on patient´s experiences of the intervention
Self-careBaseline, 3 and 6 monthsAssessed 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
AppetiteBaseline, 3 and 6 monthsAssessed 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
Thirst distressBaseline, 3 and 6 monthsAssessed 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
Subjective physical activityBaseline, 3 and 6 monthsAssessed by the instrument titled International Physical Activity Questionnaire (IPAQ). Measure the minutes of physical activity during a day.
Objective physical activityBaseline, 3 and 6 monthsMeasured with a non-invasive miniature electronic logger during 4-5 days per time frame

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026