Adherence Trial With MS LifeLines ® Services

Stopped early

Conditions studied: Multiple Sclerosis, Relapsing-Remitting

In brief

This is a Phase IV study to compare the current level of MS LifeLines ® (MSLL) services (face-to-face nursing visits and phone contacts) with customized MSLL services, to determine the optimal services to enhance medication adherence and treatment persistence with Rebif ® subcutaneous three times a week.

Key facts

Study ID

NCT01905527

Run by

EMD Serono

People needed

306

Starts

2013-07-01

Expected to finish

2015-01-01

Last updated by the study team

2015-02-02

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 to 65 years at the time of informed consent signature
• Male or female
• Female subjects of child bearing potential who report they are not pregnant at screening and agree to avoid pregnancy during study participation by using adequate contraception, defined as two barrier methods, one barrier method with a spermicide, intrauterine device, or use of oral female contraceptive
• Outpatient status at time of online screening
• Subjects prescribed Rebif by their treating physicians as the first disease-modifying drug (DMD) they have received, or up to one prior treatment with either Rebif, Copaxone ®, Avonex ® , Extavia ®, Betaseron ®, Gilenya™, and Aubagio ® (with accelerated elimination), Tysabri ® and Tecfidera™
• Access to, and ability to use, a computer, a mouse, the internet, and an email address. In addition, subjects in the Group A will be required to have access to a telephone that accepts text messaging (in case randomized to the Custom subgroup)
• Subject-reported ability to complete online assignments and read English
• Electronically verified informed consent before any trial-related activities are carried out

You may not qualify if…

• Any combination therapy with another DMD for Multiple Sclerosis (MS) while participating in the trial
• Score of 4 on any of the items of the MSRS-R or a score between 5 and 8, inclusive, on the PDDS
• Surgical intervention planned during the 12-month study period
• Pregnant or breastfeeding. Note subjects who are 90 days postpartum, stable, and do not breastfeed may participate.
• History of malignancy, with the exception of skin cancer completely excised and considered cured;
• History of seizures or unexplained blackouts within 30 days prior to online screening
• Current illegal drug use at the time of online screening;
• Any prior participation in an interventional clinical trial for MS (except for Aubagio ® or Tecfidera™), participation in any trial within 30 days prior to online screening, or current participation in another clinical trial;
• Current treatment of another autoimmune disorder other than stable thyroid disease at the time of online screening
• History of prior treatment for MS with any of the following: alemtuzumab, cyclophosphamide, methotrexate, azathioprine, cyclosporin, intravenous immunoglobulin (IVIg), and plasma exchange
• Other significant subject-reported disease that would exclude the subject from the trial
• Significant renal or hepatic impairment that would compromise completion of the trial

Where it is running

• Call EMD Serono Medical Information for information on recruiting sites — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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