NCT Number: NCT03216616
Guided Self-Management Intervention Targeting Fatigue in Rheumatic Inflammatory Diseases
Fatigue is common and debilitating in rheumatic inflammatory diseases as for other chronical medical conditions. The purpose of this study is to develope and evaluate a cognitive behavioural intervention targeting fatigue. The aim of the intervention is to improve fatigue self-management by changing behavioral and cognitive factors contributing to perceived fatigue. Levels of fatigue, depressive symptoms and self esteem will be measured before, after and three months after the intervention.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Men and women over 18 years with inflammatory rheumatic diseases and fatigue at Department of Rheumatology, Diakonhjemmet Hospital
Exclusion criteria
- Unable to provide informed consent
- Unable to read and understand Norwegian
- Unable to complete a survey
Treatment and study plan
Primary outcomes
-
Screening of the perceived level of fatigue in patients with inflammatory rheumatic disease
Time frame: 2-10 minutes
Patients with rheumatic inflammatory diseases suffering from fatigue will be asked to complete the Chalder Fatigue Questionnaire
-
Screening of depressive symptoms in patients with inflammatory rheumatic disease and fatigue
Time frame: 2-10 minutes
Patients with rheumatic inflammatory diseases suffering from fatigue will be asked to complete the Patient Health Questionnaire-9 (PHQ-9)
-
Screening of the patients perceived self efficacy in coping with fatigue
Time frame: 10-15 minutes
The patients will be asked to answer questions about fatigue, activity and rest, sleep problems, worrying and rumination.
-
Reduce perceived fatigue and increase perceived self efficacy in relation to coping with fatigue in patients with inflammatory rheumatic diseases
Time frame: 6 weeks-6 months
Patients enrolled in the study will attend a course or an individual treatment with a clinical psychologist aimed to reduce symptoms of fatigue and improve their self efficacy by means of Cognitive Behaviour Therapy (CBT)
-
Detection of changes in perceived levels of fatigue
Time frame: 2-10 minutes
Patients will be asked to complete the Chalder Fatigue Questionnaire one month and three months after receiving CBT. Results will be compared to the scores obtained prior to CBT.
-
Detection of changes in symptoms of depression
Time frame: 2-10 minutes
The patients will be asked to complete the Patient Health Questionnaire-9 (PHQ-9) one month and three months after receiving CBT. Results will be compared to the scores obtained prior to CBT.
-
Detection of changes in the patients perceived self efficacy in coping with fatigue
Time frame: 10-15 minutes
The patients will be asked to answer questions about fatigue, activity and rest, sleep problems, worrying and rumination one month and three months after receiving CBT. Results will be compared to the scores obtained prior to CBT.
Sponsors and collaborators
Lead sponsor
Diakonhjemmet Hospital
Other
Collaborators
- Extrastiftelsen
- Norsk revmatikerforbund
Registry information
Important dates
- Study start
- 2014
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- Jul 13, 2017
- Registry last updated
- Jul 13, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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