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Lupus Intervention for Fatigue Trial (LIFT)

Primary Purpose

Fatigue, Physical Activity, Lupus Erythematosus, Systemic

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Experimental
Control
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fatigue focused on measuring Fatigue, Physical Activity, Lupus

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • include meeting at least 4 of 11 American College of Rheumatology (ACR) classification criteria for definite SLE, or 3 out of 11 ACR classification criteria with also meeting at least one SLICC criteria
  • be at least 18 years of age
  • have a BMI between 18-40 kg/m2
  • be able to ambulate at least household distances (50ft)
  • be able to provide informed consent.
  • be able to speak and read English

Exclusion criteria:

  • include pregnancy at baseline
  • not meeting inclusion criteria.

Sites / Locations

  • Holly MilaegerRecruiting
  • Northwestern UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention

Control

Arm Description

The experimental intervention is a unique combination of four individual counseling sessions based in motivational interviewing focusing on physical activity, dietary behavior and behavioral strategies. The individual sessions will provide a tailored personalized intervention including problem-solving and goal setting for increasing physical activity, and following a healthy diet. Healthy Lifestyle Coaches (RN or MPH) will be responsible for conducting the individual for a caseload of participants. There are no drugs involved in the intervention.

The control group intervention will receive four individual phone calls checking in with participants regarding questions about the study or from the educational sessions focusing on SLE disease management, each lasting approximately 10-15 minutes.

Outcomes

Primary Outcome Measures

Change in Fatigue Severity Scale over time
Online questionnaire

Secondary Outcome Measures

Change in Physical Activity Scale over time
Accelerometry
Change in International Physical Activity Questionnaire (IPAQ) over time
Phone Interview Questionnaire
Godin Leisure Time Exercise Questionnaire
Phone Interview Questionnaire

Full Information

First Posted
January 7, 2016
Last Updated
January 12, 2023
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT02653287
Brief Title
Lupus Intervention for Fatigue Trial
Acronym
LIFT
Official Title
Lupus Intervention for Fatigue Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

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

5. Study Description

Brief Summary
Participants in the Chicago Lupus Database or individuals seen at Northwestern Medicine will be approached to enroll in a one year clinical trial looking at decreasing fatigue in persons with systemic lupus erythematosus (SLE). The intervention group will receive individual coaching sessions focusing on physical activity and nutrition while the control group will receive individual calls in relation to SLE self-management educational sessions.This study is designed to evaluate the LIFT intervention to decrease fatigue (primary outcome), improve physical activity (secondary outcome) and dietary behavior (exploratory outcome) in persons with SLE.
Detailed Description
Participants in the Chicago Lupus Database or individuals seen at Northwestern Medicine will be approached to enroll in a one year clinical trial looking at decreasing fatigue in persons with systemic lupus erythematosus (SLE). The intervention group will receive individual coaching based in motivational interviewing sessions focusing on physical activity and nutrition while the control group will receive individual calls focusing on SLE self-management. This study is designed to evaluate the LIFT intervention to decreased fatigue (primary outcome), improve physical activity (secondary outcome) and dietary behavior (exploratory outcome) in persons with SLE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatigue, Physical Activity, Lupus Erythematosus, Systemic
Keywords
Fatigue, Physical Activity, Lupus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
The experimental intervention is a unique combination of four individual counseling sessions based in motivational interviewing focusing on physical activity, dietary behavior and behavioral strategies. The individual sessions will provide a tailored personalized intervention including problem-solving and goal setting for increasing physical activity, and following a healthy diet. Healthy Lifestyle Coaches (RN or MPH) will be responsible for conducting the individual for a caseload of participants. There are no drugs involved in the intervention.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
The control group intervention will receive four individual phone calls checking in with participants regarding questions about the study or from the educational sessions focusing on SLE disease management, each lasting approximately 10-15 minutes.
Intervention Type
Behavioral
Intervention Name(s)
Experimental
Intervention Description
The experimental intervention includes 4 individual coaching sessions (initial 1 hour in-person and remaining 10-15 minutes per telephone) designed to identify barriers and supports for physical activity and nutrition using motivational interviewing. They occur shortly after randomization, 1.5, 3, and 6 months. Daily participants monitor their physical activity via the Fitbit Flex and their dietary behavior on a paper diary.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
The control group will receive four individual phone calls focusing on education for SLE disease management, as well as answering any questions the participants have about the study. Topics include: what is lupus, laboratory tests, medications, taking charge of your health care and managing stress (2 sessions). Each call will last about 10-15 minutes, and occur shortly after randomization, then at 1.5, 3, and 6 months.
Primary Outcome Measure Information:
Title
Change in Fatigue Severity Scale over time
Description
Online questionnaire
Time Frame
Baseline, 3, 6, 12 months
Secondary Outcome Measure Information:
Title
Change in Physical Activity Scale over time
Description
Accelerometry
Time Frame
Baseline, 3, 6, 12 months
Title
Change in International Physical Activity Questionnaire (IPAQ) over time
Description
Phone Interview Questionnaire
Time Frame
Baseline, 3, 6, 12 months
Title
Godin Leisure Time Exercise Questionnaire
Description
Phone Interview Questionnaire
Time Frame
Baseline, 6, 12 months
Other Pre-specified Outcome Measures:
Title
Change in Nutrition Data Systems for Research (NDSR) over time
Description
Dietary Recall Interview
Time Frame
Baseline, 6, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: include meeting at least 4 of 11 American College of Rheumatology (ACR) classification criteria for definite SLE, or 3 out of 11 ACR classification criteria with also meeting at least one SLICC criteria be at least 18 years of age have a BMI between 18-40 kg/m2 be able to ambulate at least household distances (50ft) be able to provide informed consent. be able to speak and read English Exclusion criteria: include pregnancy at baseline not meeting inclusion criteria.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dominique Kinnett-Hopkins, PhD
Phone
312-503-0869
Email
dominique.kinnett-hopkins@northwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Linda Ehrlich-Jones, PhD, RN
Phone
312-238-0743
Email
ljones1@sralab.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosalind Ramsey-Goldman, MD, DrPH
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Holly Milaeger
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Holly Milaeger, MPH
Phone
312-503-1919
Email
holly.milaeger@northwestern.edu
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dominique Kinnett-Hopkins, PhD
Phone
312-503-0869
Email
dominique.kinnett-hopkins@northwestern.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
It is the intent of all investigators in this project to share any and all resources generated as a result of an award for this project. The final data from this project will be de-identified in accordance with HIPAA guidelines.
Citations:
PubMed Identifier
20656619
Citation
Ramsey-Goldman R, Rothrock N. Fatigue in systemic lupus erythematosus and rheumatoid arthritis. PM R. 2010 May;2(5):384-92. doi: 10.1016/j.pmrj.2010.03.026.
Results Reference
background
PubMed Identifier
26238554
Citation
del Pino-Sedeno T, Trujillo-Martin MM, Ruiz-Irastorza G, Cuellar-Pompa L, de Pascual-Medina AM, Serrano-Aguilar P; Spanish Systemic Lupus Erythematosus CPG Development Group. Effectiveness of Nonpharmacologic Interventions for Decreasing Fatigue in Adults With Systemic Lupus Erythematosus: A Systematic Review. Arthritis Care Res (Hoboken). 2016 Jan;68(1):141-8. doi: 10.1002/acr.22675.
Results Reference
background
PubMed Identifier
25251755
Citation
Ahn GE, Chmiel JS, Dunlop DD, Helenowski IB, Semanik PA, Song J, Ainsworth B, Chang RW, Ramsey-Goldman R. Self-reported and objectively measured physical activity in adults with systemic lupus erythematosus. Arthritis Care Res (Hoboken). 2015 May;67(5):701-7. doi: 10.1002/acr.22480.
Results Reference
background
PubMed Identifier
21183562
Citation
Mancuso CA, Perna M, Sargent AB, Salmon JE. Perceptions and measurements of physical activity in patients with systemic lupus erythematosus. Lupus. 2011 Mar;20(3):231-42. doi: 10.1177/0961203310383737. Epub 2010 Dec 23.
Results Reference
background
PubMed Identifier
14635294
Citation
Ramsey-Goldman R, Schilling EM, Dunlop D, Langman C, Greenland P, Thomas RJ, Chang RW. A pilot study on the effects of exercise in patients with systemic lupus erythematosus. Arthritis Care Res. 2000 Oct;13(5):262-9. doi: 10.1002/1529-0131(200010)13:53.0.co;2-8.
Results Reference
background
PubMed Identifier
22311939
Citation
Davies RJ, Lomer MC, Yeo SI, Avloniti K, Sangle SR, D'Cruz DP. Weight loss and improvements in fatigue in systemic lupus erythematosus: a controlled trial of a low glycaemic index diet versus a calorie restricted diet in patients treated with corticosteroids. Lupus. 2012 May;21(6):649-55. doi: 10.1177/0961203312436854. Epub 2012 Feb 6.
Results Reference
background
PubMed Identifier
21135297
Citation
Lin JS, O'Connor E, Whitlock EP, Beil TL. Behavioral counseling to promote physical activity and a healthful diet to prevent cardiovascular disease in adults: a systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2010 Dec 7;153(11):736-50. doi: 10.7326/0003-4819-153-11-201012070-00007.
Results Reference
background
PubMed Identifier
20456590
Citation
Delahanty LM. Research charting a course for evidence-based clinical dietetic practice in diabetes. J Hum Nutr Diet. 2010 Aug;23(4):360-70. doi: 10.1111/j.1365-277X.2010.01065.x. Epub 2010 Apr 27.
Results Reference
background
PubMed Identifier
2803071
Citation
Krupp LB, LaRocca NG, Muir-Nash J, Steinberg AD. The fatigue severity scale. Application to patients with multiple sclerosis and systemic lupus erythematosus. Arch Neurol. 1989 Oct;46(10):1121-3. doi: 10.1001/archneur.1989.00520460115022.
Results Reference
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Lupus Intervention for Fatigue Trial

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