Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma

Before the research starts (screening): After signing this consent form, the participant
will be asked some questions to find out if the participant can be in the research study:

- A medical history, which includes questions about the participant's physical and mental
health, current medications, and any allergies.

If these tests show that the participant are eligible to participate in the research study,
the participant will receive the study intervention. If the participant does not meet the
eligibility criteria, the participant will not be able to participate in this research
study.

- After the screening procedures confirm that the participant is eligible to participate
in the research study:

- Collections Visit One: After the screening visit confirms that the participant is
eligible to participate, the participant will be scheduled for Collections Visit One.
At Collections Visit One, the participant will complete:

- A demographic questionnaire: This will include questions about the participant's age,
gender and ethnicity.

- A series of questionnaires: These will ask the participant's about their overall
wellness and take about 30-45 minutes to complete.

- A small blood sample collection: Trained nursing staff will take about 1.5 tablespoons
of blood from a single prick to the participant's arm. This procedure will take about
10-15 minutes. This is to provide samples for research tests that may help the
investigator's learn more about how the study treatment affects how the participant's
genes are expressed.

- OPTIONAL - Bone marrow, plasma and serum collection: This collection is optional and is
described in more detail in Section O. Trained nursing staff will take about 1
tablespoon of bone marrow through a standard bone marrow aspirate procedure. This
procedure takes about 20-30 minutes to complete, however most of the time is used to
get everything ready (such as preparing the skin) as well as 5-10 minutes reserved for
relaxing after the procedure is completed. This is to provide samples for research
tests that may help the investigator learn more about how the study treatment affects
the participant's disease. (This collection is optional and is described in more detail
in section O.)

- Since the effect of the study intervention with other medications may not be known, it
is important that the participant tell the research doctor about all prescription and
non-prescription drugs, herbal preparations and nutritional supplements that the
participant is taking or is planning to take.

- Randomization: In order to measure the effects of the intervention, the participant
will be "randomized" into one of the study groups after Collections

- Visit One: Immediate Group or Waitlist Control. The Immediate Group will receive the
study intervention within two weeks after the Screening and Collections Visit One
procedures. Randomization means that the participant is put into a group by chance. It
is like flipping a coin. The participant will have an equal chance of being placed in
either group. Both groups will receive the same intervention during the course of the
study, but at different time points.

- If the participant is assigned to the Waitlist Control group, Collections Visit One
will be followed by 3 months of waiting for the intervention. The participant would
then attend Collections Visit Two, followed by the intervention (3 months) and then by
Collections Visit Three.

- If the participant is assigned to the Immediate Group, Collections Visit One will be
followed by the intervention (3 months). the participant would then attend Collections
Visit Two, followed by 3 months of continuing to practice what the participant learned
during the intervention, and then by Collections Visit Three.

- After Collections Visit One, the participant will be given a group assignment and a
calendar of future study visits indicating the potential date, time and locations of
the participant's study visits.

- Study Intervention: The intervention will consist of one intake with a psychologist
(approximately 60 minutes), 8 3RP sessions once a week over the course of 8 weeks
(approximately 1 hour and 30 minutes each), and one exit visit (approximately 30
minutes) over the course of 3-months. All intervention visits will take place at the
Benson-Henry Institute for Mind Body Medicine at Massachusetts General Hospital.

- During the intervention (and follow up period for those in the Immediate Group), the
participant will be asked to practice what the participant has learned in the
intervention by listening to a 20-minute audio CD daily. Additionally, the participant
will be asked to keep track of their daily practice by filling out an online or paper
log. During the 3RP session, the clinician will address any barriers or problems the
participant may be having with the daily practice and help to problem solve them with
the participant.

- Collections Visit Two: This visit will be the same as Collections Visit One.

- Collections Visit Three: During this visit, the participant will complete:

- A series of questionnaires: These will ask about the participant's overall wellness,
and will take about 30-45 minutes to complete.

- A small blood sample collection: Trained nursing staff will take about 1.5 tablespoons
of blood from a single prick to your arm. This procedure takes about 10-15 minutes.
This is to provide samples for research tests that may help the investigators learn
more about how the study treatment affects how the participant's genes are expressed.

- The investigators will also collect information regarding any changes in the
participants medical history since their last visit.

Research Study Plan:

Immediate Group

- Screening Visit: Week 1

- Collections Visit One: Week 1 or 2

- 3RP Session One: Week 3

- 3RP Session Two: Week 4

- 3RP Session Three: Week 5

- 3RP Session Four: Week 6

- 3RP Session Five: Week 7

- 3RP Session Six: Week 8

- 3RP Session Seven: Week 9

- 3RP Session Eight: Week 10

- Collections Visit Two: Week 11/12

- Follow Up Period (home practice): Weeks 13-21 Collections Visit Three: Week 22-24

Waitlist Control

- Screening Visit: Week 1

- Collections Visit One: Week 1 or 2

- Waiting Period: Weeks 2-10

- Collections Visit Two: Week 11 or 12

- 3RP Session One: Week 13

- 3RP Session Two: Week 14

- 3RP Session Four: Week 15

- 3RP Session Five: Week 16

- 3RP Session Six: Week 17

- 3RP Session Seven: Week 18

- 3RP Session Eight: Week 19

- Collections Visit Three: Week 22, 23, or 24

- Planned Follow-up (Immediate Group Only): The investigator would like to keep track of
the participant's home practice and medical condition for 12 weeks after completion of
the 3RP intervention. The investigator would like to do this by contacting the
participant by e-mail or phone once a month to see how the participant is doing. By
Keeping in touch with the participant and checking on their practice and condition
every month helps the investigator look at the long-term effects of the research study.
At the end of the 12 weeks, the participant will come in for their last study visit -
the follow up visit, which is described above.

Inclusion Criteria:

- Participants must have confirmed high-risk monoclonal gammopathy of undetermined
significance (MGUS) or smoldering multiple myeloma (SMM) as defined below in table #.

MGUS

- Serum monoclonal protein level < 3 g/dL but > 1.5g/dl,

- Bone marrow plasma cells < 10%

- Non-IgG MGUS (ie IgA, IgM, IgD MGUS)

- Abnormal serum free light chain ratio (ie ratio of kappt to lambda free light chains
< 0.26 or > 1.65)

- Absence of end-organ damage, such as lytic bone lesions, anemia, hypercalcemia, or
renal failure, that can be attributed to a plasma cell proliferative disorder

SMM (also referred to as asymptomatic multiple myeloma)

- Serum monoclonal protein (IgG or IgA) level > 3 g/dL,

- and /or bone marrow plasma cells > 10%,

- absence of end-organ damage, such as lytic bone lesions, anemia, hypercalcemia, or
renal failure, that can be attributed to a plasma cell proliferative disorder

- Participants must be at least 18 years old. Because no dosing or adverse event data
are currently available on the use of RR in participants <18 years of age, children
are excluded from this study.

- The effects of RR on the developing human fetus are unknown. For this reason, should
a woman become pregnant or suspect she is pregnant while participating in this study,
she should inform her treating physician immediately.

- Ability to understand and the willingness to sign a written informed consent
document.

Exclusion Criteria:

- Participants who exhibit any of the following conditions at screening will not be
eligible for admission into the study.

- Participants with concurrent active cancer or active cancer with in the last 5 years
are ineligible.

- Participants with serious or unstable illness, as determined by study physicians and
clinicians, may be deemed unfit to participate.

- Participants with current bipolar or psychotic disorders with active symptoms or
treatment within the last 5 year will be excluded.

- Participants will be excluded if they are currently taking (within the last 6 months)
psychoactive medications (e.g. mood stabilizers, antipsychotics), with the exception
of hypnotics and antidepressants, which will be permitted.

- Participants may not be receiving any other study agents.