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Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus: The Living Well With Lupus Study

Primary Purpose

Systemic Lupus Erythematosus

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Living well with Lupus
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Lupus Erythematosus focused on measuring Life style, Behavioral intervention, Cardiovascular risk, Life quality

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Living well with Lupus Group

    Usual Care Group

    Arm Description

    A newly developed intervention focused on promoting lifestyle change through recommendations for structured and unstructured physical activity and healthy eating.

    This group will receive all regular medical care and advice healthy

    Outcomes

    Primary Outcome Measures

    Risk cardiovascular score
    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.

    Secondary Outcome Measures

    Body mass index (BMI)
    assessed by weight (kg) and height (m) that will be combined to report BMI in kg/m^2
    Waist circumference (cm)
    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
    assessed by blood sample analysis and combined to determine lipid profile
    Insulin sensitivity
    assessed by oral glucose tolerance test (OGTT)
    Systolic and Diastolic blood pressure
    assessed by auscultatory method with mercury sphygmomanometer
    Physical activity level
    assessed by thigh-mounted accelerometer (ActivPAL™ micro)
    Food consumption
    assessed by three 24-hour food recall in non-consecutive days (being one of the days on the weekend)
    Visceral fat
    assessed by tomography
    Peak oxygen consumption, as assessed by a cardiopulmonary exercise test
    Endothelial function
    assessed by flow-mediated vasodilatation (FMD)
    Disease activity
    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
    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
    assessed by the Visual Analogic Scale (0 and 10 scale). Higher values represent worst global health status.
    Patients' perceptions of the intervention
    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]
    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]
    score ranges from 40 to 280 with higher scores represent worst life quality.
    Physical functioning assessed by Timed-Stands
    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
    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
    Patients will be instructed to squeeze the dynamometer as hard as possible
    Fatigue
    assessed by Fatigue Scale (FACIT). The final score can vary from 0 to 52, where higher final score representing higher level of fatigue.
    Anxiety
    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
    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)
    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)
    assessed by analysis of blood sample
    Erythrocyte sedimentation rate
    assessed by analysis of blood sample
    Inflammatory markers (blood biochemistry)
    assessed by serum cytokines

    Full Information

    First Posted
    February 18, 2020
    Last Updated
    June 10, 2020
    Sponsor
    University of Sao Paulo
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04431167
    Brief Title
    Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus: The Living Well With Lupus Study
    Official Title
    Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus With High Cardiovascular Risk: The Living Well With Lupus Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 1, 2020 (Anticipated)
    Primary Completion Date
    December 1, 2022 (Anticipated)
    Study Completion Date
    December 1, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Sao Paulo

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This research program aims to investigate the clinical, physiological, metabolic and molecular effects of lifestyle change in patients with systemic lupus erythematosus with high cardiovascular risk. This 6-month parallel-group randomized controlled trial aims to investigate the feasibility and efficacy of a newly developed lifestyle change intervention - through recommendations for structured and unstructured physical activity and healthy eating - on increasing physical activity level and improving eating habits. Potential effects of the intervention on cardiovascular and cardiometabolic risk factors, health-related quality of life, symptoms of anxiety and depression, sleep quality and immune function will be investigated. Gold-standard techniques and a variety of analyses will be performed to access the potential mechanisms involved in response to this intervention.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Systemic Lupus Erythematosus
    Keywords
    Life style, Behavioral intervention, Cardiovascular risk, Life quality

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Experimental group and no intervention group (usual care group)
    Masking
    Outcomes Assessor
    Masking Description
    The researcher responsible for performing the blood flow measurement will be blinded to the allocation of groups
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Living well with Lupus Group
    Arm Type
    Experimental
    Arm Description
    A newly developed intervention focused on promoting lifestyle change through recommendations for structured and unstructured physical activity and healthy eating.
    Arm Title
    Usual Care Group
    Arm Type
    No Intervention
    Arm Description
    This group will receive all regular medical care and advice healthy
    Intervention Type
    Behavioral
    Intervention Name(s)
    Living well with Lupus
    Intervention Description
    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.
    Primary Outcome Measure Information:
    Title
    Risk cardiovascular score
    Description
    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.
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Body mass index (BMI)
    Description
    assessed by weight (kg) and height (m) that will be combined to report BMI in kg/m^2
    Time Frame
    6 months
    Title
    Waist circumference (cm)
    Description
    assessed by measuring tape positioned at the midpoint between the last floating vertebra and the iliac crest.
    Time Frame
    6 months
    Title
    Total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides
    Description
    assessed by blood sample analysis and combined to determine lipid profile
    Time Frame
    6 months
    Title
    Insulin sensitivity
    Description
    assessed by oral glucose tolerance test (OGTT)
    Time Frame
    6 months
    Title
    Systolic and Diastolic blood pressure
    Description
    assessed by auscultatory method with mercury sphygmomanometer
    Time Frame
    6 months
    Title
    Physical activity level
    Description
    assessed by thigh-mounted accelerometer (ActivPAL™ micro)
    Time Frame
    6 months
    Title
    Food consumption
    Description
    assessed by three 24-hour food recall in non-consecutive days (being one of the days on the weekend)
    Time Frame
    6 months
    Title
    Visceral fat
    Description
    assessed by tomography
    Time Frame
    6 months
    Title
    Peak oxygen consumption, as assessed by a cardiopulmonary exercise test
    Time Frame
    6 months
    Title
    Endothelial function
    Description
    assessed by flow-mediated vasodilatation (FMD)
    Time Frame
    6 months
    Title
    Disease activity
    Description
    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.
    Time Frame
    6 months
    Title
    Damage index
    Description
    assessed by Systemic Lupus International Collaborating Clinics/ American College of Rheumatology - Damage Index. Total score range from 0 (no damage) to 46 (maximum damage).
    Time Frame
    6 months
    Title
    Global health status
    Description
    assessed by the Visual Analogic Scale (0 and 10 scale). Higher values represent worst global health status.
    Time Frame
    6 months
    Title
    Patients' perceptions of the intervention
    Description
    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.
    Time Frame
    6 months
    Title
    Quality of Life assesment assessed by the Short-Form Health Survey-36 (SF36) [followed by its scale information in the Description]
    Description
    maximum score is 100, with higher scores representing better life quality
    Time Frame
    6 months
    Title
    Quality of Life assessed by Systemic Lupus Erythematosus Quality of Life Questionnaire ( SLEQOL) [followed by its scale information in the Description]
    Description
    score ranges from 40 to 280 with higher scores represent worst life quality.
    Time Frame
    6 months
    Title
    Physical functioning assessed by Timed-Stands
    Description
    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
    Time Frame
    6 months
    Title
    Physical functioning assessed by Timed Up-and-Go
    Description
    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
    Time Frame
    6 months
    Title
    Physical functioning assessed by handgrip test
    Description
    Patients will be instructed to squeeze the dynamometer as hard as possible
    Time Frame
    6 months
    Title
    Fatigue
    Description
    assessed by Fatigue Scale (FACIT). The final score can vary from 0 to 52, where higher final score representing higher level of fatigue.
    Time Frame
    6 months
    Title
    Anxiety
    Description
    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.
    Time Frame
    6 months
    Title
    Depression
    Description
    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.
    Time Frame
    6 months
    Title
    Sleep quality assessed by data obtained from Actigraph (Actigraph GT3x)
    Description
    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.
    Time Frame
    6 months
    Title
    C-reactive protein (PCR)
    Description
    assessed by analysis of blood sample
    Time Frame
    6 months
    Title
    Erythrocyte sedimentation rate
    Description
    assessed by analysis of blood sample
    Time Frame
    6 months
    Title
    Inflammatory markers (blood biochemistry)
    Description
    assessed by serum cytokines
    Time Frame
    6 months

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Gender Eligibility Description
    Only female participants will be eligible
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 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 Exclusion Criteria: 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
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Bruno Gualano, PhD
    Phone
    +551130618789
    Email
    gualano@usp.br

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    we can share the individual data of the participants if the request is reasonable

    Learn more about this trial

    Healthy Lifestyle Intervention in Patients With Systemic Lupus Erythematosus: The Living Well With Lupus Study

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