Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus: The Living Well With Lupus Study
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|ClinicalTrials.gov Identifier: NCT04431167|
Recruitment Status : Unknown
Verified June 2020 by Bruno Gualano, University of Sao Paulo.
Recruitment status was: Not yet recruiting
First Posted : June 16, 2020
Last Update Posted : June 16, 2020
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|Condition or disease||Intervention/treatment||Phase|
|Systemic Lupus Erythematosus||Behavioral: Living well with Lupus||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||80 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||Experimental group and no intervention group (usual care group)|
|Masking:||Single (Outcomes Assessor)|
|Masking Description:||The researcher responsible for performing the blood flow measurement will be blinded to the allocation of groups|
|Official Title:||Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus With High Cardiovascular Risk: The Living Well With Lupus Study|
|Estimated Study Start Date :||September 1, 2020|
|Estimated Primary Completion Date :||December 1, 2022|
|Estimated Study Completion Date :||December 1, 2022|
Experimental: Living well with Lupus Group
A newly developed intervention focused on promoting lifestyle change through recommendations for structured and unstructured physical activity and healthy eating.
Behavioral: Living well with Lupus
The lifestyle change intervention will involve two constructs: increasing the level of physical activity and improving eating habits, each with its own specific domains and goals. It will be based on a structured program of physical exercises and selection of individualized goals in the domains of transportation, leisure and work to reduce sedentary behavior with the aim of increasing the level of physical activity, as well as establishing changes in dietary aspects, involving consumption domains, structure, behavior and eating attitude using nutritional counseling techniques.
No Intervention: Usual Care Group
This group will receive all regular medical care and advice healthy
- Risk cardiovascular score [ Time Frame: 6 months ]assessed by measures of five standard variables (HDL cholesterol, triglycerides, fasting blood glucose, waist circumference and blood pressure - average of systolic and diastolic blood pressures). Z-score = [(50 - HDL cholesterol)/sd + (triglycerides - 150)/ sd] + [(fasting blood glucose - 100)/ sd] + [(waist circumference - 88)/ sd] + [(blood pressure - 115)/ sd]. Higher score values represent higher risk. *sd: standard deviation. Higher Z-score represent higher risk.
- Body mass index (BMI) [ Time Frame: 6 months ]assessed by weight (kg) and height (m) that will be combined to report BMI in kg/m^2
- Waist circumference (cm) [ Time Frame: 6 months ]assessed by measuring tape positioned at the midpoint between the last floating vertebra and the iliac crest.
- Total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides [ Time Frame: 6 months ]assessed by blood sample analysis and combined to determine lipid profile
- Insulin sensitivity [ Time Frame: 6 months ]assessed by oral glucose tolerance test (OGTT)
- Systolic and Diastolic blood pressure [ Time Frame: 6 months ]assessed by auscultatory method with mercury sphygmomanometer
- Physical activity level [ Time Frame: 6 months ]assessed by thigh-mounted accelerometer (ActivPAL™ micro)
- Food consumption [ Time Frame: 6 months ]assessed by three 24-hour food recall in non-consecutive days (being one of the days on the weekend)
- Visceral fat [ Time Frame: 6 months ]assessed by tomography
- Peak oxygen consumption, as assessed by a cardiopulmonary exercise test [ Time Frame: 6 months ]
- Endothelial function [ Time Frame: 6 months ]assessed by flow-mediated vasodilatation (FMD)
- Disease activity [ Time Frame: 6 months ]The activity of the disease, which will be impaired by safety, will be assessed by the presence of anti-dsDNA, using the ELISA technique and confirmation by indirect immunofluorescence in Crithidia luciliae and assessed by the questionnaire Systemic lupus erythematosus disease activity index 2000 (SLEDAI-2000). Total score ranges from 0 to 105. Higher scores represent higher disease activity.
- Damage index [ Time Frame: 6 months ]assessed by Systemic Lupus International Collaborating Clinics/ American College of Rheumatology - Damage Index. Total score range from 0 (no damage) to 46 (maximum damage).
- Global health status [ Time Frame: 6 months ]assessed by the Visual Analogic Scale (0 and 10 scale). Higher values represent worst global health status.
- Patients' perceptions of the intervention [ Time Frame: 6 months ]assessed by focus group. A semi-structured script composed of open questions about intervention positive and negative points, barriers for physical activity practice and changes in food consumption, perceptions of health improvement or worsening (physical and psychological aspects), well-being, motivation to maintain the changes made, perspectives regarding health and disease.
- Quality of Life assesment assessed by the Short-Form Health Survey-36 (SF36) [followed by its scale information in the Description] [ Time Frame: 6 months ]maximum score is 100, with higher scores representing better life quality
- Quality of Life assessed by Systemic Lupus Erythematosus Quality of Life Questionnaire ( SLEQOL) [followed by its scale information in the Description] [ Time Frame: 6 months ]score ranges from 40 to 280 with higher scores represent worst life quality.
- Physical functioning assessed by Timed-Stands [ Time Frame: 6 months ]evaluates the maximum number of stand-ups that a subject could perform from a standard height (i.e., 45 cm) armless chair within 30 s
- Physical functioning assessed by Timed Up-and-Go [ Time Frame: 6 months ]evaluates the time required for the subject to rise from a standard arm chair, walk towards a line drawn on the floor three meters away, turn, return, and sit back down again
- Physical functioning assessed by handgrip test [ Time Frame: 6 months ]Patients will be instructed to squeeze the dynamometer as hard as possible
- Fatigue [ Time Frame: 6 months ]assessed by Fatigue Scale (FACIT). The final score can vary from 0 to 52, where higher final score representing higher level of fatigue.
- Anxiety [ Time Frame: 6 months ]assessed by sub-scale of Hospital Anxiety and Depression Scale (HADS), called HADS-A. Total score ranges from 0 to 21. Where higher final score representing higher level.
- Depression [ Time Frame: 6 months ]assessed by sub-scale of Hospital Anxiety and Depression Scale (HADS), called HADS-D. Total score ranges from 0 to 21. Where higher final score representing higher level.
- Sleep quality assessed by data obtained from Actigraph (Actigraph GT3x) [ Time Frame: 6 months ]Data from actigraph will come as these measures: Total Sleep Time (hours/day), Sleep Efficiency (%), Sleep Onset Latency (min), and Wake After Sleep Onset (min), and this data will be considered to determine the sleep quality.
- C-reactive protein (PCR) [ Time Frame: 6 months ]assessed by analysis of blood sample
- Erythrocyte sedimentation rate [ Time Frame: 6 months ]assessed by analysis of blood sample
- Inflammatory markers (blood biochemistry) [ Time Frame: 6 months ]assessed by serum cytokines
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|Ages Eligible for Study:||18 Years to 65 Years (Adult, Older Adult)|
|Sexes Eligible for Study:||Female|
|Gender Based Eligibility:||Yes|
|Gender Eligibility Description:||Only female participants will be eligible|
|Accepts Healthy Volunteers:||No|
- Women between 18 and 65 years old diagnosed with systemic lupus erythematosus
- one or more high cardiovascular risk factors
- SLEDAI score ≤ 4
- Treatment with prednisone at a dosage <10 mg/d and treatment with hydroxychloroquine in a stable dose
- another rheumatic diseases (except for secondary Sjogren's syndrome)
- participation in structured exercise training programs and/or prescriptive diets
- illiterate or with diagnosed cognitive disorders or musculoskeletal impairments that potentially compromise understanding and participation in the intervention
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04431167
|Contact: Bruno Gualano, PhDemail@example.com|
|Responsible Party:||Bruno Gualano, Professor, University of Sao Paulo|
|Other Study ID Numbers:||
Living well with lupus Study
|First Posted:||June 16, 2020 Key Record Dates|
|Last Update Posted:||June 16, 2020|
|Last Verified:||June 2020|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||Yes|
|Plan Description:||we can share the individual data of the participants if the request is reasonable|
|Studies a U.S. FDA-regulated Drug Product:||No|
|Studies a U.S. FDA-regulated Device Product:||No|
Lupus Erythematosus, Systemic
Connective Tissue Diseases
Immune System Diseases