- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06443268
Cerebrovascular Disease: Quality of Life (CODE: QoL) (CODE:QoL)
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Anton Schmick, MD
- Phone Number: +41442551111
- Email: anton.schmick@usz.ch
Study Contact Backup
- Name: Susanne Wegener, MD
- Phone Number: +41442551111
- Email: susanne.wegener@usz.ch
Study Locations
-
-
Zurich
-
Zürich, Zurich, Switzerland, 8091
- Recruiting
- Department of Neurology, University Hospital Zurich
-
Contact:
- Anton Schmick, MD
- Email: anton.schmick@usz.ch
-
Contact:
- Susanne Wegener, MD
- Email: susanne.wegener@usz.ch
-
Sub-Investigator:
- Schmick Anton, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
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
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:
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:
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
Score is sum of answer values (1 + 2 + 3); Range: 0-21 Scoring Categories
|
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
|
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
|
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)
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
Sponsor
Investigators
- Principal Investigator: Susanne Wegener, MD, University of Zurich
Publications and helpful links
General Publications
- MAHONEY FI, BARTHEL DW. FUNCTIONAL EVALUATION: THE BARTHEL INDEX. Md State Med J. 1965 Feb;14:61-5. No abstract available.
- Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001 Sep;16(9):606-13. doi: 10.1046/j.1525-1497.2001.016009606.x.
- Haley WE, Roth DL, Hovater M, Clay OJ. Long-term impact of stroke on family caregiver well-being: a population-based case-control study. Neurology. 2015 Mar 31;84(13):1323-9. doi: 10.1212/WNL.0000000000001418. Epub 2015 Mar 4.
- Avery K, Donovan J, Peters TJ, Shaw C, Gotoh M, Abrams P. ICIQ: a brief and robust measure for evaluating the symptoms and impact of urinary incontinence. Neurourol Urodyn. 2004;23(4):322-30. doi: 10.1002/nau.20041.
- van Swieten JC, Koudstaal PJ, Visser MC, Schouten HJ, van Gijn J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1988 May;19(5):604-7. doi: 10.1161/01.str.19.5.604.
- HAMILTON M. The assessment of anxiety states by rating. Br J Med Psychol. 1959;32(1):50-5. doi: 10.1111/j.2044-8341.1959.tb00467.x. No abstract available.
- Sharpley CF, McFarlane JR, Slominski A. Stress-linked cortisol concentrations in hair: what we know and what we need to know. Rev Neurosci. 2011 Dec 8;23(1):111-21. doi: 10.1515/RNS.2011.058.
- Brott T, Adams HP Jr, Olinger CP, Marler JR, Barsan WG, Biller J, Spilker J, Holleran R, Eberle R, Hertzberg V, et al. Measurements of acute cerebral infarction: a clinical examination scale. Stroke. 1989 Jul;20(7):864-70. doi: 10.1161/01.str.20.7.864.
- Bullinger M. German translation and psychometric testing of the SF-36 Health Survey: preliminary results from the IQOLA Project. International Quality of Life Assessment. Soc Sci Med. 1995 Nov;41(10):1359-66. doi: 10.1016/0277-9536(95)00115-n.
- Hinz A, Klein AM, Brahler E, Glaesmer H, Luck T, Riedel-Heller SG, Wirkner K, Hilbert A. Psychometric evaluation of the Generalized Anxiety Disorder Screener GAD-7, based on a large German general population sample. J Affect Disord. 2017 Mar 1;210:338-344. doi: 10.1016/j.jad.2016.12.012. Epub 2016 Dec 18.
- Ma X, Zhang J, Zhong W, Shu C, Wang F, Wen J, Zhou M, Sang Y, Jiang Y, Liu L. The diagnostic role of a short screening tool--the distress thermometer: a meta-analysis. Support Care Cancer. 2014 Jul;22(7):1741-55. doi: 10.1007/s00520-014-2143-1. Epub 2014 Feb 8.
- Bundesamt für Statistik. Herz und Kreislauf Erkrankungen [online; visited: 21.11.2022] https://www.bfs.admin.ch/bfs/de/home/statistiken/gesundheit/gesundheitszustand/krankheiten/herz-kreislauf-erkrankungen.html
- Costa TF, Gomes TM, Viana LR, Martins KP, Costa KN. Stroke: patient characteristics and quality of life of caregivers. Rev Bras Enferm. 2016 Sep-Oct;69(5):933-939. doi: 10.1590/0034-7167-2015-0064. English, Portuguese.
- Zhang J, Lee DT. Meaning in stroke family caregiving: A literature review. Geriatr Nurs. 2017 Jan-Feb;38(1):48-56. doi: 10.1016/j.gerinurse.2016.07.005. Epub 2016 Sep 23.
- Jeong YG, Myong JP, Koo JW. The modifying role of caregiver burden on predictors of quality of life of caregivers of hospitalized chronic stroke patients. Disabil Health J. 2015 Oct;8(4):619-25. doi: 10.1016/j.dhjo.2015.05.005. Epub 2015 May 29.
- Hansel M, Steigmiller K, Luft AR, Gebhard C, Held U, Wegener S. Neurovascular disease in Switzerland: 10-year trends show non-traditional risk factors on the rise and higher exposure in women. Eur J Neurol. 2022 Sep;29(9):2851-2860. doi: 10.1111/ene.15434. Epub 2022 Jun 22.
- Schmick A, Juergensen M, Rohde V, Katalinic A, Waldmann A. Assessing health-related quality of life in urology - a survey of 4500 German urologists. BMC Urol. 2017 Jun 19;17(1):46. doi: 10.1186/s12894-017-0235-1.
- Hamann J, Herzog L, Wehrli C, Dobrocky T, Bink A, Piccirelli M, Panos L, Kaesmacher J, Fischer U, Stippich C, Luft AR, Gralla J, Arnold M, Wiest R, Sick B, Wegener S. Machine-learning-based outcome prediction in stroke patients with middle cerebral artery-M1 occlusions and early thrombectomy. Eur J Neurol. 2021 Apr;28(4):1234-1243. doi: 10.1111/ene.14651. Epub 2020 Dec 21.
- Muller MJ. Development and retest reliability of a German version of the Sexual Behaviour Questionnaire (SBQ-G). Arch Androl. 2007 Mar-Apr;53(2):67-9. doi: 10.1080/01485010600915186.
- Reis D, Lehr D, Heber E, Ebert DD. The German Version of the Perceived Stress Scale (PSS-10): Evaluation of Dimensionality, Validity, and Measurement Invariance With Exploratory and Confirmatory Bifactor Modeling. Assessment. 2019 Oct;26(7):1246-1259. doi: 10.1177/1073191117715731. Epub 2017 Jun 18.
- Kim JH, Kim O. Influence of mastery and sexual frequency on depression in Korean men after a stroke. J Psychosom Res. 2008 Dec;65(6):565-9. doi: 10.1016/j.jpsychores.2008.06.005. Epub 2008 Oct 28.
- Oyewole OO, Ogunlana MO, Gbiri CAO, Oritogun KS. Prevalence and impact of disability and sexual dysfunction on Health-Related Quality of Life of Nigerian stroke survivors. Disabil Rehabil. 2017 Oct;39(20):2081-2086. doi: 10.1080/09638288.2016.1219395. Epub 2016 Aug 22.
- Forsberg-Warleby G, Moller A, Blomstrand C. Life satisfaction in spouses of patients with stroke during the first year after stroke. J Rehabil Med. 2004 Jan;36(1):4-11. doi: 10.1080/16501970310015191.
- Kjork E, Blomstrand C, Carlsson G, Lundgren-Nilsson A, Gustafsson C. Daily life consequences, cognitive impairment, and fatigue after transient ischemic attack. Acta Neurol Scand. 2016 Feb;133(2):103-110. doi: 10.1111/ane.12435. Epub 2015 May 8.
- Tarlow, B. J., Wisniewski, S. R., Belle, S. H., Rubert, M., Ory, M. G., & Gallagher-Thompson, D. (2004). Positive Aspects of Caregiving: Contributions of the REACH Project to the Development of New Measures for Alzheimer's Caregiving. Research on Aging, 26(4), 429-453. https://doi.org/10.1177/0164027504264493
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Behavioral Symptoms
- Mental Disorders
- Pathologic Processes
- Cardiovascular Diseases
- Vascular Diseases
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Urologic Diseases
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Urination Disorders
- Stress, Psychological
- Brain Ischemia
- Intracranial Hemorrhages
- Elimination Disorders
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Stroke
- Urinary Incontinence
- Ischemic Attack, Transient
- Hemorrhage
- Cerebral Hemorrhage
- Enuresis
- Cerebrovascular Disorders
- Caregiver Burden
Other Study ID Numbers
- 2023-00224
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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