LIFT: Lupus Intervention for Fatigue Trial

Sponsor
Northwestern University (Other)
Overall Status
Recruiting
CT.gov ID
NCT02653287
Collaborator
(none)
200
2
2
49
100
2

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Experimental
  • Other: Control
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Lupus Intervention for Fatigue Trial
Actual Study Start Date :
May 1, 2019
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

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.

Behavioral: Experimental
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.

Active Comparator: Control

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.

Other: Control
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.

Outcome Measures

Primary Outcome Measures

  1. Change in Fatigue Severity Scale over time [Baseline, 3, 6, 12 months]

    Online questionnaire

Secondary Outcome Measures

  1. Change in Physical Activity Scale over time [Baseline, 3, 6, 12 months]

    Accelerometry

  2. Change in International Physical Activity Questionnaire (IPAQ) over time [Baseline, 3, 6, 12 months]

    Phone Interview Questionnaire

  3. Godin Leisure Time Exercise Questionnaire [Baseline, 6, 12 months]

    Phone Interview Questionnaire

Other Outcome Measures

  1. Change in Nutrition Data Systems for Research (NDSR) over time [Baseline, 6, 12 months]

    Dietary Recall Interview

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Holly Milaeger Chicago Illinois United States 60611
2 Northwestern University Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University

Investigators

  • Principal Investigator: Rosalind Ramsey-Goldman, MD, DrPH, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Rosalind Ramsey-Goldman, Professor, Northwestern University
ClinicalTrials.gov Identifier:
NCT02653287
Other Study ID Numbers:
  • LIFT Study
First Posted:
Jan 12, 2016
Last Update Posted:
Mar 4, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rosalind Ramsey-Goldman, Professor, Northwestern University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 4, 2022