Cerebrovascular Disease: Quality of Life (CODE: QoL) (CODE:QoL)

May 29, 2024 updated by: Susanne Wegener, University of Zurich

The goal of this observational study is to learn about quality of life, stress and caregiver burden in patients with stroke and their caregivers.

The main question is:

• to discover the factors associated with quality of life and stress in patient-caregiver dyads.

Participants will be asked to fill out questionnaires and agree to provide a hair sample (in order to measure stress hormones in hair) and consent to use of their routine clinical and laboratory data.

Researchers will compare a group of participants without stroke to establish a comparable baseline.

Study Overview

Detailed Description

Introduction/Background

In Switzerland, approximately 21,000 people suffer a stroke each year. Stroke causes neurological impairments for those affected and brings about a sudden change in their life situation. The relatives of stroke patients receive new social roles and are challenged in a new way by the morbidity of the affected person, leading to a change in their quality of life and aggravation of stress. Unlike chronic diseases, a stroke occurs suddenly, so relatives have no opportunity to gradually adapt to the new living circumstances or to deal with the new psychosocial roles and demands beforehand. To what extent the daily life of patients and their relatives changes and what impact this has on their quality of life and stress has not been systematically investigated in Switzerland thus far.

Aims and significance of the project

The aim of the project is to systematically assess the quality of life and stress, as well as to capture stress biomarkers in stroke patients and their relatives. The investigators plan to conduct sequential measurements of quality of life and stress hormones at multiple time points over 12 months. The goal is in particular to uncover the relationships between the extent of patients' impairments, their quality of life, and stress in affected individuals and their relatives. This is a first-time project with the goal of learning more about stressors and biological relationships. This will create the basis for a multimodal intervention to improve the quality of life of those affected and their relatives, which will be investigated in a follow-up project.

Methods

The Investigators plan a prospective study with a survey of stroke patients and their relatives regarding their quality of life in everyday life. It will also be examined, how multiple stress biomarkers (which will be determined in blood and hair) are related to quality of life and stress and which clinical factors have a positive and negative influence on the well-being of patients and their relatives.

Study Type

Observational

Enrollment (Estimated)

680

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Zurich
      • Zürich, Zurich, Switzerland, 8091
        • Recruiting
        • Department of Neurology, University Hospital Zurich
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Schmick Anton, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Control group:

We will include 40 patients without previous stroke OR patients with a minor stroke > 3 years ago and no sustained significant disability (mRS 0 or 1) along with their close relative (to simulate informal caregivers) (total 80 participants).

Main group:

We will include 300 patients and informal caregivers with a first cerebrovascular event treated at our clinic > 18 years. The caregivers will be defined as the closest person to the patient with the most contact. (total 600 participants)

Description

Control group:

Inclusion criteria:

  • over 18 years old
  • No previous stroke OR previous stroke >3 years ago
  • No significant disability (maximum mRS 1)
  • ambulatory patients at the University Hospital of Zurich (USZ), Dept. of Neurology
  • Patients' AND caregiver's ability to give informed consent
  • Patients' AND close relative's / caregiver's willingness to participate

Exclusion criteria:

• Medication with steroid hormones (prednisone, prednisolone, dexamethasone, methylprednisolone, hydrocortisone etc.) within last 3 months

Main Group:

Inclusion criteria:

  • over 18 years old
  • Patients diagnosed with either transient ischemic attack, ischemic stroke or intracerebral hemorrhage and their caregivers
  • Caregiver of a patient as described above, age over 18 years
  • Hospitalized or ambulatory patients at the University Hospital of Zurich (USZ) included within 28 days from event.
  • Patients' AND caregiver's ability to give informed consent
  • Patients' AND caregiver's willingness to participate

Exclusion criteria:

• Medication with steroid hormones (prednisone, prednisolone, dexamethasone, methylprednisolone, hydrocortisone etc.) within last 3 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients with ischemic / hemorrhagic stroke, transient ischemic attack, intracerebral hemorrhage
The following parameters will be sequentially assessed in caregivers and patients (baseline, at 3 months and at 12 months): 1) quality of life / functioning will be determined through questionnaires (SF-36, EQ-5DL, ECOG (Eastern Cooperative Oncology Group) / Karnofsky, Barthel Index, ICIQ) 2) stress levels & anxiety levels, caregiver burden will be assessed by the following questionnaires: Distress Thermometer, SBQ-G, GAD-7, PHQ-9, PSS-10, ZBI, PAC. Cortisol will be measured in hair to indicate stress within the past 3 months [18]. Fasting glucose, lipid profiles and HbA1c along with blood count, sodium, potassium, creatinine, TSH (thyroid-stimulating hormone) will be measured in routine blood samples from patients at the time of clinical checkups. Blood pressure, pulse and BMI will be determined during clinical visit in patients and additionally in caregivers.
Caregivers of patients described above
Caregivers of patients with ischemic / hemorrhagic stroke, transient ischemic attack, intracerebral hemorrhage
The following parameters will be sequentially assessed in caregivers and patients (baseline, at 3 months and at 12 months): 1) quality of life / functioning will be determined through questionnaires (SF-36, EQ-5DL, ECOG (Eastern Cooperative Oncology Group) / Karnofsky, Barthel Index, ICIQ) 2) stress levels & anxiety levels, caregiver burden will be assessed by the following questionnaires: Distress Thermometer, SBQ-G, GAD-7, PHQ-9, PSS-10, ZBI, PAC. Cortisol will be measured in hair to indicate stress within the past 3 months [18]. Fasting glucose, lipid profiles and HbA1c along with blood count, sodium, potassium, creatinine, TSH (thyroid-stimulating hormone) will be measured in routine blood samples from patients at the time of clinical checkups. Blood pressure, pulse and BMI will be determined during clinical visit in patients and additionally in caregivers.
Patients WITHOUT ischemic / hemorrhagic stroke, transient ischemic attack, intracerebral hemorrhage
Patients WITHOUT ischemic / hemorrhagic stroke, transient ischemic attack, intracerebral hemorrhage or with an event > 3 years ago AND no disability
The following parameters will be sequentially assessed in caregivers and patients (baseline, at 3 months and at 12 months): 1) quality of life / functioning will be determined through questionnaires (SF-36, EQ-5DL, ECOG (Eastern Cooperative Oncology Group) / Karnofsky, Barthel Index, ICIQ) 2) stress levels & anxiety levels, caregiver burden will be assessed by the following questionnaires: Distress Thermometer, SBQ-G, GAD-7, PHQ-9, PSS-10, ZBI, PAC. Cortisol will be measured in hair to indicate stress within the past 3 months [18]. Fasting glucose, lipid profiles and HbA1c along with blood count, sodium, potassium, creatinine, TSH (thyroid-stimulating hormone) will be measured in routine blood samples from patients at the time of clinical checkups. Blood pressure, pulse and BMI will be determined during clinical visit in patients and additionally in caregivers.
Caregivers of patients above
may include close relatives
The following parameters will be sequentially assessed in caregivers and patients (baseline, at 3 months and at 12 months): 1) quality of life / functioning will be determined through questionnaires (SF-36, EQ-5DL, ECOG (Eastern Cooperative Oncology Group) / Karnofsky, Barthel Index, ICIQ) 2) stress levels & anxiety levels, caregiver burden will be assessed by the following questionnaires: Distress Thermometer, SBQ-G, GAD-7, PHQ-9, PSS-10, ZBI, PAC. Cortisol will be measured in hair to indicate stress within the past 3 months [18]. Fasting glucose, lipid profiles and HbA1c along with blood count, sodium, potassium, creatinine, TSH (thyroid-stimulating hormone) will be measured in routine blood samples from patients at the time of clinical checkups. Blood pressure, pulse and BMI will be determined during clinical visit in patients and additionally in caregivers.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of Life as assessed via Short Form - 36 (SF-36)
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Short Form - 36 (SF-36)

Multi-item scale with 8 domains assessing health related quality of life:

  • limitations in physical activities
  • limitations in social activities
  • limitations in usual role activities because
  • pain
  • limitations in social role activities
  • vitality
  • overall mental health
  • overall health

Domains are scored seperately; Values span from 0 to 100, higher values indicate fewer limitations

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stress
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

as assessed using Perceived Stress Scale - 10 (PSS-10)

Scoring is based on 2 subscales:

Subscale 1: Perceived self-efficacy (PSE), range: (4-20)

Subscale 2: Perceived helplessness (PH), range: (6-30)

Total score PSS-10 is evaluated by adding both sub scale scores.

Values span from 10 to 50, higher values indicate higher levels of stress

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Positive Aspects of Caregiving:
Time Frame: caregivers at 0, 3 and 12 months after cerebrovascular event.

Measure of caregiver burden

Questionnaire: 11 items / Likert scales (1-5)

Values span from 11 to 55, higher values indicate positive aspects of caregiving

caregivers at 0, 3 and 12 months after cerebrovascular event.
Zarit Burden Interview:
Time Frame: caregivers at 0, 3 and 12 months after cerebrovascular event.

Measure of caregiver burden

22 items / Likert scales (0-4) Values span from 0 to 88, higher values indicate higher caregiver burden

caregivers at 0, 3 and 12 months after cerebrovascular event.
Stroke Related Quality of Life
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Stroke Impact Scale 3.0 (SIS-3.0)

SIS-3.0 includes 60 items and assesses 9 domains using Likert scales:

  • Strength - 4 items
  • Hand function - 5 items
  • Activities of daily living - 10 items
  • Mobility - 9 items
  • Communication - 7 items
  • Emotion - 9 items
  • Memory and thinking - 7 items
  • Participation/Role function - 8 items
  • Perceived recovery since stroke onset - single-item VAS (visual analog scale)

Domains are scored seperately; Values span from 0 to 100, higher values indicate fewer limitations

patients at 0, 3 and 12 months after cerebrovascular event.
Anxiety
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using General Anxiety Disorder- (GAD-7)

7 items / Likert scales (0-3) Values span from 0 to 21, higher values indicate higher level of anxiety and functional impairment

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Depression
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Patient Health Questionnaire - 9 (PHQ-9)

9 items, evaluated by likert scale (0-3) Values span from 0 to 27, higher values indicate higher probability of depression and decreased functional status

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Sexual Quality of Life
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Sexual Behavior Questionnaire German (SBQ-G)

Equal base questions (1-6) and gender specific questions m(7-11), f(7-10)

Single item evaluation with two answer categories

(0-1) dysfunctional (2-3) functional

Evaluation of MGISD (Mean Global Index of sexual Dysfunction): Arithmetic mean of 1,4,5,6,8f/11m

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Incontinence
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using International Consultation on Incontinence Questionnaire (ICIQ)

3 Questions regarding urinary incontinence

  • Frequency?
  • Severity?
  • Impact on quality of life?

Score is sum of answer values (1 + 2 + 3); Range: 0-21

Scoring Categories

  • slight (1-5)
  • moderate (6-12)
  • severe (13-18)
  • very severe (19-21)
caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
neurological functioning of the patients (NIHSS)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using National Institutes of Health Stroke Scale (NIHSS)

NIHSS

  • 13 assessed functional domains
  • Range 0-42, higher score indicates severe impairment
patients at 0, 3 and 12 months after cerebrovascular event.
neurological functioning of the patients (mRS)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using modified Rankin Scale (mRS)

mRS

• Range: (0-6) 0 = no symptoms, 6 = death, higher score indicates severe impairment

patients at 0, 3 and 12 months after cerebrovascular event.
neurological functioning of the patients (Barthel Index)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Barthel Index

Barthel Index

  • Physical impairment in daily life / self-care
  • score ranges from 0-100
  • higher score indicates fewer limitations
patients at 0, 3 and 12 months after cerebrovascular event.
Distress
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using Distress Thermometer

Assessment with Visual Analog Scale (0-10), higher scale indicates more distress.

Selection of aspects in life causing distress

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Quality of Life (short)
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using EuroQol-5 (EQ5-DL)

Evaluation of 5 different aspects of health with likert scale (1-5)

  • MOBILITY
  • SELF-CARE
  • USUAL ACTIVITIES
  • PAIN / DISCOMFORT
  • ANXIETY / DEPRESSION

Each domain is scored individually, higher values indicate higher impairment of quality of life

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Quality of Life (short)
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

will be assessed using EuroQol-5 (EQ5-DL)

Visual analog scale:

EQ VAS 0-100, higher score indicates better perceived current health

caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
cortisol / cortisone in hair (pg/mg)
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
fasting glucose (mmol/l)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
patients at 0, 3 and 12 months after cerebrovascular event.
HbA1c (in %)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
patients at 0, 3 and 12 months after cerebrovascular event.
Lipid profiles (LDL, HDL, triglycerides in mmol/l)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
patients at 0, 3 and 12 months after cerebrovascular event.
TSH (mU/l)
Time Frame: patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
patients at 0, 3 and 12 months after cerebrovascular event.
Blood pressure (systolic & diastolic in mmHg)
Time Frame: caregivers and patients at 0, 3 and 12 months after cerebrovascular event.
Stress biomarkers
caregivers and patients at 0, 3 and 12 months after cerebrovascular event.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Susanne Wegener, MD, University of Zurich

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 27, 2023

Primary Completion (Estimated)

April 30, 2028

Study Completion (Estimated)

June 30, 2028

Study Registration Dates

First Submitted

May 4, 2024

First Submitted That Met QC Criteria

May 29, 2024

First Posted (Actual)

June 5, 2024

Study Record Updates

Last Update Posted (Actual)

June 5, 2024

Last Update Submitted That Met QC Criteria

May 29, 2024

Last Verified

May 1, 2024

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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