Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT00424099 |
| Other study ID # |
2005-0613 |
| Secondary ID |
R01NR010162-01A1 |
| Status |
Completed |
| Phase |
Phase 2/Phase 3
|
| First received |
|
| Last updated |
|
| Start date |
January 9, 2007 |
| Est. completion date |
November 22, 2021 |
Study information
| Verified date |
May 2023 |
| Source |
M.D. Anderson Cancer Center |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The goal of this clinical research study is to learn if methylphenidate (Ritalin) can help to
control fatigue caused by cancer. Its effect on other symptoms such as drowsiness,
depression, sleeplessness, physical activity, and anxiety will also be studied. Another goal
of this study is to learn if receiving a phone call by a nurse improves fatigue in patients.
Description:
Fatigue is one of the most common problems in patients with advanced cancer. Currently, there
are no treatments for managing fatigue. Methylphenidate is a stimulant that increases ability
to pay attention, increases mental alertness, and decreases feelings of fatigue.
If you are found to be eligible to take part in this study, you will be randomly assigned (as
in the roll of dice) to one of 4 groups. You will have an equal chance of being placed in any
of the 4 groups. You, the medical staff, and researchers will not know to which group you
have been assigned.
Regardless of which group you are in, you will record your fatigue in a daily diary at
breakfast, lunch, dinner, and before bedtime. Based on your level of fatigue, you will take
the study drug as needed. You can take the study drug every 2 hours but you may not take more
than 4 capsules a day.
Participants in Group 1 will take a methylphenidate capsule by mouth as needed to relieve
symptoms of fatigue for 14 days. A nurse will call you 4-6 times in the first two weeks to
ask about side effects and other symptoms. The phone calls should take about 10-20 minutes.
The study nurse will set up a convenient time for you to take the phone call.
Participants in Group 2 will take a placebo capsule by mouth as needed for 14 days. A placebo
is a capsule that does not contain any medication but looks just like the methylphenidate. A
nurse will call you 4-6 times in the first two weeks to ask about side effects and other
symptoms. The phone calls should take about 10-20 minutes. The study nurse will set up a
convenient time for you to take the phone call.
Participants in Group 3 will take a methylphenidate capsule by mouth as needed for 14 days.
Participants in this group will not receive any calls from a study nurse. However, A research
staff member will call you 4-6 times in the first two weeks to ask about side effects and
other symptoms. The phone calls should take about 10-20 minutes. The research staff member
will set up a convenient time for you to take the phone call.
Participants in Group 4 will take a placebo capsule by mouth as needed for 14 days.
Participants in this group will not receive any calls from a study nurse. However, A research
staff member will call you 4-6 times in the first two weeks to ask about side effects and
other symptoms. The phone calls should take about 10-20 minutes. The research staff member
will set up a convenient time for you to take the phone call.
You will be asked to wear a wrist actigraph monitor (a wristwatch that keeps track of your
physical activity and your sleep cycles) for the first 14 days.
You will keep a daily diary of your fatigue and other symptoms, the number and times pills
are taken, and your fatigue rating before and 2 hours after taking methylphenidate.
On about day 15 (or within 3 days) you will return to the palliative care clinic at M. D.
Anderson for tests. You will be asked about your level of drowsiness, pain, constipation, and
fatigue. You will be asked about any side effects you may have experienced and the
effectiveness of the drug. You will repeat the 6 minute physical test, the cognitive status
test, and you will return the actigraph monitor to the research nurse. You will also be given
the option to receive up to 4 capsules of methylphenidate per day until Day 36. You will not
be told whether you were taking placebo or methylphenidate during Days 1-14. If you cannot
come to the clinic on Day 15, all tests except the walking test, may be performed over the
telephone. You will be asked to mail the actigraph back.
If you decide not to take methylphenidate on Days 15-36, you will be considered off-study and
you will have end-of-study tests on Day 15. If you decide to take methylphenidate on Days
15-36, you will remain on study until Day 36. On Day 36, you will have end-of-study tests.
For end-of-study tests, you will repeat the physical and cognitive tests. You will be asked
about your symptoms and any side effects you may be experiencing. You will then return to
your primary physician who will discuss with you whether or not to continue on the
methylphenidate based on your response to the drug.
Your participation in this study should end on either Day 15 or Day 36. However, if you
develop intolerable side effects (including fatigue) while on this study, the medication will
be stopped and you will be removed from the study.
This is an investigational study. Methylphenidate has been approved by the FDA and is a
commercially available drug. It is FDA approved at this dose level. Its use in this study,
for this purpose, is investigational. About 212 patients will take part in this multicenter
study. About 142 patients will be enrolled at The University of Texas (UT) MD Anderson.
