- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04324320
Psychological Distress in Outpatient Oncological Rehabilitation
Study Overview
Status
Intervention / Treatment
Detailed Description
Psychological distress in cancer patients is higher than in the average population and is associated with a lower health-related quality of life. In the course of the disease and its treatment, a psychological distress reaction can lead to a psychosocial crisis and a mental disorder that requires treatment. On average, 25% of all cancer patients suffer from depression, anxiety or adjustment disorders at any point in the course of their disease, and an average of 32% of all cancer patients express the need for psychosocial support. With an increasing reduction in inpatient length of stay times, outpatient care gains growing importance in the context of psycho-oncological diagnostics and aftercare. The overlap between physical symptoms due to cancer diagnosis and treatment and physical symptoms that are related to psychological burdens requires sensitive psycho-oncological diagnostics. This should be carried out as early as possible in the course of the disease so that existing psychological distress can be recognized early and thus a progression of the symptoms can be prevented.
The study aims to assess psychological distress and co-morbidity as well as relevant sociodemographic, anthropometric, medical and functional data in patients treated at the Outpatient Clinic for Oncological Rehabilitation at the Department of Physical Medicine, Rehabilitation and Occupational Medicine at the Medical University of Vienna.
Results should serve as a basis for further individual treatment recommendations.
By ascertaining the psychological distress, appropriate support and treatment measures can be recommended to the patients at an early stage, which help to improve the symptoms, enable participation and thus improve the quality of life of the patients. The assessment of the current individual need for psychological care also helps to refer patients to an inpatient oncological rehabilitation setting that provides the care that is needed more appropriately.
Results should also improve the psychological care of oncologic patients in general. Based on the findings, the psychological care offered within the framework of the current outpatient and inpatient oncological rehabilitation setting could be adapted and expanded as necessary. The results of the study should serve to integrate psycho-oncological care into the overall outpatient oncological rehabilitation concept.
A monocentric cross-sectional study is to be carried out on 165 patients with malignant tumour diseases as well as benign central nervous system tumours over a period of approximately 2 years.
Medical assessment of sociodemographic, anthropometric, medical and functional data will be performed. The gained information is also relevant for physical therapy prescription and treatment recommendations given by the physiatrist at the outpatient clinic for oncological rehabilitation.
Psychological distress and the need for psycho-oncological care for outpatients is determined through standardized screening and suitable assessment procedures. Patients will receive an immediate therapy recommendation regarding their psychological complaints by the clinical psychologist and psychotherapist who performs the assessment.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Barbara Wagner, MD
- Phone Number: +43-1-40400-43300
- Email: barbara.wagner@meduniwien.ac.at
Study Contact Backup
- Name: Margarete Steiner, MSc
- Phone Number: +43-1-40400-43300
- Email: margarete.steiner@meduniwien.ac.at
Study Locations
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Vienna, Austria, 1090
- Medical University of Vienna
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Contact:
- Barbara Wagner, MD
- Phone Number: +43 1 40400 43300
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Contact:
- Margarete Steiner, MSc
- Phone Number: +43 1 40400 43300
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Principal Investigator:
- Richard Crevenna, Prof MD MBA MMSc
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Sub-Investigator:
- Margarete Steiner, MSc
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Sub-Investigator:
- Barbara Wagner, MD
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Sub-Investigator:
- Galateja Jordakieva, MD PhD
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Sub-Investigator:
- Dominikus Huber, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with malignant tumour diseases and benign CNS tumours who present to the Outpatient Clinic for Oncological Rehabilitation at the Department of Physical Medicine, Rehabilitation and Occupational Medicine at the Medical University of Vienna
- patients who agree to participate in the study
Exclusion Criteria:
- bad physical condition that does not enable the patient to participate in the study
- language barriers (insufficient understanding of the German language)
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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outpatients (oncological rehabilitation)
the population studied in this cross-sectional study includes patients with malignant tumour diseases and benign CNS tumours who present to the Outpatient Clinic for Oncological Rehabilitation at the Department of Physical Medicine and Rehabilitation of the Medical University of Vienna
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medical assessment includes the collection of
psychological assessment includes several standardized screening and assessment questionnaires and tools:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
anxiety, depression, stress: HADS-D
Time Frame: 5 minutes
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HADS-D is a validated screening tool (questionnaire) to assess anxiety and depression in patients with physical and psychological disorders, especially taking into account a physical primary disease.
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5 minutes
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
anthropometric data (weight, height, body mass index)
Time Frame: 3 minutes
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weight, height and body mass index are measured
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3 minutes
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Psycho-oncologic basis assessment (PO-BADO)
Time Frame: 25-30 minutes
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The PO-BADO is a rating scale to assess the subjectively perceived stress in oncologic patients.
The assessment is performed by a physician.
Sociodemographic and medical data as well as psychologic distress are evaluated.
Further relevant sociodemographic and medical data is assessed by a physician.
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25-30 minutes
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Visual analog scale (VAS)
Time Frame: 2 minutes
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The visual analog scale is a semiquantitative test to assess subjective pain intensity on a scale between 0-10 (0 being no pain at all, 10 being the worst pain imaginable).
The patient is asked to report the most intense pain within the last week that is associated with the cancer diagnosis/treatment as well as musculoskeletal pain.
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2 minutes
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functional assessment: hand grip strength
Time Frame: 5 minutes
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Hand grip strength measures the maximal isometric handgrip strength using a JAMAR®dynamometer (in kilograms).
Assessment is performed in a standardized position, sitting on a chair, elbow is flexed 90 degrees, upper extremity is in neutral position.
3 assessments are performed with the dominant hand, the mean value is registered.
The motoric skill strength is assessed.
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5 minutes
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functional assessment: 6 Minute Walking Test
Time Frame: 8 minutes
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The 6 Minute Walking Test (6MWT) is used to estimate the basic motoric function endurance.
It helps to evaluate the patients cardiovascular and pulmonal performance below the anerobic threshold.
The patient is asked to quickly walk (not run) for 6 minutes, the distance walked within 6 minutes is measured.
Walking aids and taking a break if needed is allowed.
This test has been validated and recommended for cancer patients.
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8 minutes
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functional assessment: Timed Get up and Go Test
Time Frame: 5 minutes
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Timed Get up and Go Test (TGU): this standardized test assesses functional mobility.
The patient is asked to sit on a chair with armrests.
When told, he has to get up without the help of other persons, walk a distance of 3 meters, turn and sit down again.
Walking aids such as a cane are allowed to use if necessary.
The time is registered that the person needs for that maneuver (< 10 seconds indicate no limitations in mobility).
The test has a good validity and reliability.
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5 minutes
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Quality of life: Short- Form -36
Time Frame: 10 minutes
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The Short Form -36 is a validated questionnaire to assess the health-related quality of life.
There are 8 dimensions of the test that can be summarized into the main domains "physical health" and "mental health".
Also, changes compared to the year before are evaluated.
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10 minutes
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subjective perceived stress: Perceived Stress Scale (PSS-10)
Time Frame: 5 minutes
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The PSS-10 scale measures the subjective perception of stress. 2 scales evaluate the domains "helplessness" and "self-efficacy".
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5 minutes
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resilience: resilience scale (RS-13)
Time Frame: 5 minutes
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Resilience is seen as a criterion of emotional stability and psychological health.
It is a personal resource to deal with stressful events in life.
This one-dimensional scale evaluates the resilience of a person.
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5 minutes
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fatigue: brief fatigue inventory (BFI)
Time Frame: 5 minutes
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The BFI score is a validated tool to assess cancer-related fatigue.
The questionnaire consists of 10 items that capture 6 dimensions: activity, mood, mobility, work, social relation and vitality.
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5 minutes
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disability related to pain: Pain Disability Index (PDI)
Time Frame: 5 minutes
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The PDI is used to assess the subjective impairment of a chronic pain situation in everyday life.
The questionnaire is based on a multidimensional concept of impairment due to the pain condition.
It differentiates between damage, disability and discrimination.
It evaluates 7 areas of life (family/home, recreation, social activities, work, sexuality, self-supply, vital activities.)
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5 minutes
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workability: Work Ability Index - short version (WAI-K)
Time Frame: 5 minutes
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The WAI evaluates the amount to which employed people are able to do their work in light of health, mental resources and work requirements.
It helps to estimate the individual performance regarding the current working situation.
It consists of 10 items and 7 dimensions.
The summary score is a measure for the subjective estimate of the own capacity to meet work requirements.
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5 minutes
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psychological assessment according to the diagnostic I.C.D.-10 based checklists
Time Frame: 90 minutes
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The psychological assessment is based on the results of the screening tools to identify psychosocial stress/ disorders.
It aims to further evaluate the present problems and clarify whether symptoms are subsyndromal or fulfil the criteria of a mental disorder according to the I.C.D.-10 classification.
External assessment tools used are the international diagnostic checklist for I.C.D.-10 (IDCL) and the I.C.D.-10 symptom checklist for mental disorders (SCL).
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90 minutes
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Richard Crevenna, Prof MD MBA MMSc, Medical University of Vienna
Publications and helpful links
General Publications
- Klein EM, Brahler E, Dreier M, Reinecke L, Muller KW, Schmutzer G, Wolfling K, Beutel ME. The German version of the Perceived Stress Scale - psychometric characteristics in a representative German community sample. BMC Psychiatry. 2016 May 23;16:159. doi: 10.1186/s12888-016-0875-9.
- Podsiadlo D, Richardson S. The timed "Up & Go": a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991 Feb;39(2):142-8. doi: 10.1111/j.1532-5415.1991.tb01616.x.
- Casanova C, Celli BR, Barria P, Casas A, Cote C, de Torres JP, Jardim J, Lopez MV, Marin JM, Montes de Oca M, Pinto-Plata V, Aguirre-Jaime A; Six Minute Walk Distance Project (ALAT). The 6-min walk distance in healthy subjects: reference standards from seven countries. Eur Respir J. 2011 Jan;37(1):150-6. doi: 10.1183/09031936.00194909. Epub 2010 Jun 4.
- Mehnert A, Koch U. Psychosocial care of cancer patients--international differences in definition, healthcare structures, and therapeutic approaches. Support Care Cancer. 2005 Aug;13(8):579-88. doi: 10.1007/s00520-005-0779-6. Epub 2005 Mar 1.
- Mehnert A, Lehmann C, Cao P, Koch U. [Assessment of psychosocial distress and resources in oncology--a literature review about screening measures and current developments]. Psychother Psychosom Med Psychol. 2006 Dec;56(12):462-79. doi: 10.1055/s-2006-951828. German.
- Fallowfield L, Ratcliffe D, Jenkins V, Saul J. Psychiatric morbidity and its recognition by doctors in patients with cancer. Br J Cancer. 2001 Apr 20;84(8):1011-5. doi: 10.1054/bjoc.2001.1724.
- Herschbach P, Book K, Brandl T, Keller M, Lindena G, Neuwohner K, Marten-Mittag B. Psychological distress in cancer patients assessed with an expert rating scale. Br J Cancer. 2008 Jul 8;99(1):37-43. doi: 10.1038/sj.bjc.6604420. Epub 2008 Jun 24.
- Herschbach P, Keller M, Knight L, Brandl T, Huber B, Henrich G, Marten-Mittag B. Psychological problems of cancer patients: a cancer distress screening with a cancer-specific questionnaire. Br J Cancer. 2004 Aug 2;91(3):504-11. doi: 10.1038/sj.bjc.6601986.
- Harkonen R, Harju R, Alaranta H. Accuracy of the Jamar dynamometer. J Hand Ther. 1993 Oct-Dec;6(4):259-62. doi: 10.1016/s0894-1130(12)80326-7.
- Manttari A, Suni J, Sievanen H, Husu P, Vaha-Ypya H, Valkeinen H, Tokola K, Vasankari T. Six-minute walk test: a tool for predicting maximal aerobic power (VO2 max) in healthy adults. Clin Physiol Funct Imaging. 2018 May 31. doi: 10.1111/cpf.12525. Online ahead of print.
- Schmidt K, Vogt L, Thiel C, Jager E, Banzer W. Validity of the six-minute walk test in cancer patients. Int J Sports Med. 2013 Jul;34(7):631-6. doi: 10.1055/s-0032-1323746. Epub 2013 Feb 26.
- Radbruch L, Sabatowski R, Elsner F, Everts J, Mendoza T, Cleeland C. Validation of the German version of the brief fatigue inventory. J Pain Symptom Manage. 2003 May;25(5):449-58. doi: 10.1016/s0885-3924(03)00073-3.
- van den Berg TI, Elders LA, de Zwart BC, Burdorf A. The effects of work-related and individual factors on the Work Ability Index: a systematic review. Occup Environ Med. 2009 Apr;66(4):211-20. doi: 10.1136/oem.2008.039883. Epub 2008 Nov 18.
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- 1162/2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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