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A Study on the Use of the MMF07 Foot Massager and Heat Therapy Treatments for Restless Leg Syndrome

A Randomized Prospective Study on the Efficacy of the MMF07 Foot Massager and Heat Therapy Treatments for Restless Leg Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02526277
Enrollment
28
Registered
2015-08-18
Start date
2016-01-06
Completion date
2018-09-25
Last updated
2021-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Restless Legs Syndrome

Keywords

RLS

Brief summary

The purpose of this study is to assess whether the MMF07 Foot Massager and/ or heat therapy may improve symptoms of restless legs syndrome (RLS). It will also assess the effect of the MMF07 Foot Massager and/ or heat on quality of life and sleep in people affected by RLS. Participants will be randomly assigned to one of four treatment groups; 1. MMF07 Foot Massager device 2. Heat therapy 3. Heat therapy and the MMF07 Foot Massage device 4. Neither heat nor MMF07 Foot Massager device (no treatment group)

Detailed description

Few clinical trials have looked into non-pharmacological, non-invasive treatments for restless legs syndrome, despite reports that massage, baths and vibrations can alleviate RLS symptoms. We would like to assess whether the MMF007 Foot Massager device and/or heat therapy is associated with improved severity of RLS symptoms. For this study the investigator will enroll 40 participants who have been diagnosed with restless legs syndrome, who will be followed over the course of four weeks and asked to complete two in person study visits. In the study the investigator is comparing the use of the MMF007 Foot Massager device and/ or heat therapy to a non treatment group to assess if the symptoms of RLS improve.

Interventions

DEVICEMMF07 Foot Massager
DEVICEHeat Therapy

Sponsors

MedMassager
CollaboratorUNKNOWN
Ariane Park
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Subjects between 18-75 years old diagnosed with RLS according to the diagnostic criteria of the International Restless Legs Syndrome Study Group (11) 2. Subjects should have bothersome RLS symptoms, despite best medical therapy 3. Subjects should be stable on all RLS medication for at least 4 weeks prior to enrollment 4. All subjects must have vision and be proficient in English for compliance with testing and surveys 5. All women of childbearing age must be using an acceptable form of birth control, including abstinence, intrauterine device (IUD) or intrauterine system in place for at least 3 months prior to screening, subject or partner using barrier method (e.g., condom, diaphragm, or cervical cap) with spermicide from screening through study completion; partner has a documented vasectomy \> 6 months prior to Baseline, Stable hormonal contraception (with approved oral, transdermal, or depot regimen) for at least 3 months prior to screening

Exclusion criteria

1. RLS secondary associated with end stage renal disease, iron deficiency or pregnancy 2. Concomitant sleep disorders 3. Any other condition (other than the primary indications), which in the opinion of the investigators might contribute to difficulty complying with the protocol

Design outcomes

Primary

MeasureTime frameDescription
The International Restless Legs Severity Scale4 weeksParticipants answer a series of 10 questions each of which have values ranging from 0 to 4, the points are then added together. Higher values are associated with more severe symptoms; up to a maximum severity score of 40 points and a minimum severity of 0 points.

Secondary

MeasureTime frameDescription
The Restless Legs Quality of Life Questionnaire4 weeksParticipants answer a series of 18 questions that are scored such that lower scores indicate worse quality of life. The scoring process for the RLSQoL is relatively complicated. Items 1-5, 7-10, and 13 use scales ranging from 1 to 5, with lower scores indicating a greater frequency and interference of restless legs syndrome. The total score for these items is converted to a value between 0 and 100 using an algorithm provided along with the scale. Items 6 and 16-18 require respondents to indicate how many days in the previous month or hours in the previous day they have been able to complete certain activities or have had their daily functioning interfered with. These items are scored as continuous variables (for example, ranging from 0 to 28 days for questions regarding the number of days per month). Items 11, 12, 14, and 15 are categorical variables, where a response of yes receives (a 1), a response of no receives (a 2), and a response of not applicable receives (3a).
Changes in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 44 weeksParticipants answered a series of 12 questions assessing sleep, with values ranging from 1 to 6, and an additional dichotomous indicator of optimal sleep. All items are scored so that a high score reflects more of the attribute implied by the scale name. Each item is then converted to a 0 to 100 possible range so that the lowest and highest possible scores are set at 0 and 100, respectively. In this format, scores represent the achieved percentage of the total possible score. Reference: Spritzer, K. L. & Hays, R. D. (2003, November). MOS Sleep Scale: A Manual for Use and Scoring, Version 1.0. Los Angeles, CA.

Countries

United States

Participant flow

Participants by arm

ArmCount
MMF07 Foot Massager Device
Participants randomized to the MMF07 Foot Massager device arm will be provided the MMF07 Foot Massager device and instructed to set this device at setting 3, then increase or decrease the setting to their desired level of comfort, to be used for 30 minutes at bedtime. MMF07 Foot Massager
8
Heat Therapy
Participants randomized to heat therapy will be provided an electric heating pad and will be instructed to use this pad at a medium setting for 30 minutes at bedtime. Heat Therapy
6
MMF07 Foot Massager Device and Heat Therapy
Participants randomized to both the MMF07 Foot Massager device and heat therapy will be provided both the MMF07 Foot Massager device and electric heating pad. Participants will be instructed to set the MMF07 Foot Massager device at setting 3, then increase or decrease the setting to their desired level of comfort. They will also be instructed to use the electric heating pad at a medium setting at the same time for 30 minutes at bedtime. MMF07 Foot Massager Heat Therapy
7
No Treatment
Participants receiving no intervention will be asked to not alter their nighttime routine.
7
Total28

Baseline characteristics

CharacteristicMMF07 Foot Massager DeviceHeat TherapyMMF07 Foot Massager Device and Heat TherapyNo TreatmentTotal
Age, Continuous65.8 years59.6 years59.9 years52.7 years59.6 years
Married3 Participants0 Participants2 Participants3 Participants8 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
8 Participants6 Participants7 Participants7 Participants28 Participants
RLS Severity
Mild/moderate
4 Participants3 Participants4 Participants3 Participants14 Participants
RLS Severity
Severe/very severe
4 Participants3 Participants3 Participants4 Participants14 Participants
Sex: Female, Male
Female
7 Participants3 Participants5 Participants4 Participants19 Participants
Sex: Female, Male
Male
1 Participants3 Participants2 Participants3 Participants9 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 80 / 60 / 70 / 7
other
Total, other adverse events
4 / 80 / 64 / 71 / 7
serious
Total, serious adverse events
0 / 80 / 60 / 70 / 7

Outcome results

Primary

The International Restless Legs Severity Scale

Participants answer a series of 10 questions each of which have values ranging from 0 to 4, the points are then added together. Higher values are associated with more severe symptoms; up to a maximum severity score of 40 points and a minimum severity of 0 points.

Time frame: 4 weeks

ArmMeasureValue (MEAN)Dispersion
Heat TherapyThe International Restless Legs Severity Scale17.3 score on a scaleStandard Deviation 8.1
MMF07 Foot Massager DeviceThe International Restless Legs Severity Scale12.3 score on a scaleStandard Deviation 4.2
MMF07 Foot Massager Device and Heat TherapyThe International Restless Legs Severity Scale16.9 score on a scaleStandard Deviation 6.2
No TreatmentThe International Restless Legs Severity Scale21.3 score on a scaleStandard Deviation 8.5
Secondary

Changes in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 4

Participants answered a series of 12 questions assessing sleep, with values ranging from 1 to 6, and an additional dichotomous indicator of optimal sleep. All items are scored so that a high score reflects more of the attribute implied by the scale name. Each item is then converted to a 0 to 100 possible range so that the lowest and highest possible scores are set at 0 and 100, respectively. In this format, scores represent the achieved percentage of the total possible score. Reference: Spritzer, K. L. & Hays, R. D. (2003, November). MOS Sleep Scale: A Manual for Use and Scoring, Version 1.0. Los Angeles, CA.

Time frame: 4 weeks

ArmMeasureValue (MEAN)Dispersion
Heat TherapyChanges in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 426.6 score on a scaleStandard Deviation 9.9
MMF07 Foot Massager DeviceChanges in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 431.2 score on a scaleStandard Deviation 15.8
MMF07 Foot Massager Device and Heat TherapyChanges in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 437.0 score on a scaleStandard Deviation 3.7
No TreatmentChanges in Sleep as Measured by the Medical Outcomes Sleep Study Scale at Week 448.6 score on a scaleStandard Deviation 18.4
Secondary

The Restless Legs Quality of Life Questionnaire

Participants answer a series of 18 questions that are scored such that lower scores indicate worse quality of life. The scoring process for the RLSQoL is relatively complicated. Items 1-5, 7-10, and 13 use scales ranging from 1 to 5, with lower scores indicating a greater frequency and interference of restless legs syndrome. The total score for these items is converted to a value between 0 and 100 using an algorithm provided along with the scale. Items 6 and 16-18 require respondents to indicate how many days in the previous month or hours in the previous day they have been able to complete certain activities or have had their daily functioning interfered with. These items are scored as continuous variables (for example, ranging from 0 to 28 days for questions regarding the number of days per month). Items 11, 12, 14, and 15 are categorical variables, where a response of yes receives (a 1), a response of no receives (a 2), and a response of not applicable receives (3a).

Time frame: 4 weeks

ArmMeasureValue (MEAN)Dispersion
Heat TherapyThe Restless Legs Quality of Life Questionnaire82.4 score on a scaleStandard Deviation 20.9
MMF07 Foot Massager DeviceThe Restless Legs Quality of Life Questionnaire66.7 score on a scaleStandard Deviation 25.6
MMF07 Foot Massager Device and Heat TherapyThe Restless Legs Quality of Life Questionnaire74.2 score on a scaleStandard Deviation 19.1
No TreatmentThe Restless Legs Quality of Life Questionnaire57.1 score on a scaleStandard Deviation 32.6

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026