Effect of Physical ACtivity in Fingolimod Treated patiEnts (PACE) With Relapsing-remitting Multiple Sclerosis

Phase 4

Terminated

Conditions: Fatigue in Multiple Sclerosis

Interventions: Other: Physical exercise

Registration Number: NCT01490840

Lead Sponsor: Novartis Pharmaceuticals

Brief Summary: This study evaluated the effect of an individualized web-based physical training in fingolimod -treated patients.

Detailed Description: In this study, it was planned to randomize 226 participants. However, only 178 participants were randomized during a timeframe of 2 years and 8 months. Therefore, the study was terminated due to slow enrollment and low participant compliance to the physical training schedule.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 178

Inclusion Criteria

Subjects with relapsing remitting MS defined by 2010 revised McDonald criteria
Patients with Expanded Disability Status Scale (EDSS) score of 0-3.5 (including)
Immunomodulatory treatment with prescribed fingolimod for at least one month prior to baseline
Fatigue score assessed by mFIS of equal or greater than 14 at screening
Neurologically stable with no evidence of relapse within 30 days prior to inclusion date

Exclusion Criteria

Patients who have been treated with:
- systemic corticosteroids or immunoglobulins within 1 month prior to randomization;
- immunosuppressive medications such as azathioprine, cyclophosphamide, or methotrexate within 3 months prior to randomization;
- monoclonal antibodies (including natalizumab) within 3 months prior to randomization;
- mitoxantrone within 6 months prior to randomization
- cladribine at any time.
Patients with any medically unstable condition, as assessed by the primary treating physician at each site.
Patients with any of the following cardiovascular conditions :
- history of cardiac arrest;
- history of myocardial infarction or with current unstable ischemic heart disease;
- history of angina pectoris due to coronary spasm or history of Raynaud syndrome
- Heart failure (NYHA III-IV) or any severe cardiac disease as determined by the investigator;
- history or presence of a second-degree AV block, Type II or a third-degree AV
- block
- patients receiving Class Ia (ajmaline, disopyramide, procainamide, quinidine) or
- III antiarrhythmic drugs (e.g., amiodarone, bretylium, sotalol, ibulitide, azimilide,
- dofelitide);
- proven history of sick sinus syndrome or sino-atrial heart block;
- uncontrolled hypertension
Clinically relevant internal disease (e.g. uncorrected anemia) or orthopedic diseases (e.g. scoliosis) that might interfere with physical training
Any severe disability or clinical impairment that can prevent the patient to meet all study requirements at the investigator's discretion

Other protocol-defined inclusion/exclusion criteria may apply.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Waiting	Physical exercise	Fingolimod as baseline immunomodulatory multiple sclerosis treatment is prescribed as per clinical practice. During Phase 1, participants randomized to this arm did not receive e-training exercise. After a 6 months waiting period, phase 2, participants had an introductory group session, hosted by a sports therapist. The individual training schedule was comprised of strength exercises twice a week for 30-45 minutes and endurance training once a week for 20-60 minutes for 6 months. The participants documented each training session thoroughly via the web-based application (duration, type of exercises, number of repetitions and sets, perceived exertion). A standard course of corticosteroids (methylprednisolone) on an inpatient or outpatient basis was allowed for treatment of relapses as clinically warranted. Steroid treatment consisted of 3-5 days and up to 1,000 mg methylprednisolone/day.
E-training	Physical exercise	Fingolimod as baseline immunomodulatory multiple sclerosis treatment was prescribed as per clinical practice. During phase 1, participants randomized to this arm had an introductory group session, hosted by a sports therapist. The individual training schedule was comprised of strength exercises twice a week for 30-45 minutes and endurance training once a week for 20-60 minutes for 6 months. The participants documented each training session thoroughly via the web-based application (duration, type of exercises, number of repetitions and sets, perceived exertion). A standard course of corticosteroids (methylprednisolone) on an inpatient or outpatient basis was allowed for treatment of relapses as clinically warranted. Steroid treatment consisted of 3-5 days and up to 1,000 mg methylprednisolone/day. After 6 months, Phase 2, the same Phase 1 regimen applied.

Primary Outcome Measures

Name	Time	Method
Change From Baseline in Fatigue as Measured by the Modified Fatigue Impact Scale (mFIS ).	Baseline, 6 months	The mFIS provides an assessment of the effects of fatigue in terms of physical, cognitive, and psychosocial functioning. It is a 21-item, structured, self-report questionnaire that generally can be completed with little or no intervention from an interviewer. The mFIS score ranged from 0 (not tired) to 84 (tired). A negative change from baseline indicates improvement.

Secondary Outcome Measures

Name	Time	Method
Change From Baseline in Isometric and Dynamic Muscular Strength as Measured by Sit-to-stand Test	baseline, 6 months	The Sit to Stand Test is a functional outcome measure of the lower-extremity muscle power. The test was performed 3 times with one minute rest in between. The best attempt out of three was used for the analysis. A positive change from baseline indicates improvement.
Change From Baseline in Isometric and Dynamic Muscular Strength as Measured by Change in Leg Strength and Trunk Strength	baseline, 6 months	Isometric and dynamic muscular strength was measured by an Isomed 2000 isometric measurement device (knee flexion/tension, trunk flexion/extension). Isomed 2000 device measures muscular flexion and tension under standardized training conditions. A positive change from baseline indicates improvement.
Change From Baseline in Depression as Measured by the Beck Depression Inventory Second Edition (BDI-II)	Baseline, 6 months	The Beck Depression Inventory Second Edition (BDI-II) is a 21-item self-report instrument intended to assess the existence and severity of symptoms of depression as listed in the American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders Fourth Edition. Each of the 21 items corresponding to a symptom of depression is summed to give a single score for the BDI-II. There is a four-point scale for each item ranging from 0 to 3. The total score ranges from 0 - 63. Total score of 0-13 is considered minimal range, 14-19 is mild, 20-28 is moderate, and 29-63 is severe. A negative change from baseline indicates improvement.
Change From Baseline in Aerobic Capacity (VO2max) as Measured by a Physical Endurance Spiroergometry on a Treadmill	Baseline, 6 months	Physical endurance spiroergometry was accomplished. Ergometry was assessed according to national guidelines of the German society for sports medicine. Ergometry is a combined examination of circulation and lung function and was performed as a submaximal or maximal test depending on the participant's individual performance. A negative change from baseline indicates improvement.
Change From Baseline in Peak Expiratory Flow as Measured by a Physical Endurance Spiroergometry on a Treadmill	Baseline, 6 months	Physical endurance spiroergometry was accomplished. Ergometry was assessed according to national guidelines of the German society for sports medicine. Ergometry is a combined examination of circulation and lung function and was performed as a submaximal or maximal test depending on the participant's individual performance. A positive change from baseline indicates improvement.
Change From Baseline in Quality of Life as Measured by the Hamburg Quality of Life Questionnaire in Multiple Sclerosis (HAQUAMS)	Baseline, 6 months, 12 months	The Hamburg Quality of Life Questionnaire in Multiple Sclerosis (HAQUAMS) consists of 44 items, 28 of which are the basis for computation of five subscale scores reflecting major dimensions of health-related quality of life (HRQoL) in MS: Fatigue/Thinking (4 items), Mobility lower limb (5 items), Mobility upper limb (5 items), Social function (6 items) and Mood (eight items). Subscales and total score range from 1 to 5, with high scores indicating a lower quality of life. In this study, the total score and following 3 subscales: fatigue/thinking, mobility lower limb and mobility upper limb only were analyzed. A negative change from baseline indicates improvement.
Change From Baseline in Fatigue as Measured by the WEIMuS (Würzburg Fatigue Inventory for MS)	Baseline, 6 months	The WEIMuS (Würzburg Fatigue Inventory for MS) scale is a validated self-assessment instrument to quantify the degree of fatigue. The scale consists of 17 items with 5 categories that are scored from '0' to '4'. The subscores for cognitive and physical fatigue range from 0 to 36 and from 0 to 32, respectively, with the total sum score ranging from 0 to 68; higher scores indicate higher degrees of fatigue. A negative change from baseline indicates improvement.
Change From Baseline in Isometric and Dynamic Muscular Strength as Measured by Leg Strength Endurance	baseline, 6 months	Isometric and dynamic muscular strength was measured by an Isomed 2000 isometric measurement device (knee flexion/tension, trunk flexion/extension). Isomed 2000 device measures muscular flexion and tension under standardized training conditions. A positive change from baseline indicates improvement.