Interactive Voice Response System (IVRS)
OtherTelephone based system
NCT Number: NCT00819624
The study has two goals. The first goal of the study is to compare two methods of administering questions about pain and sleep interference. The two methods being compared are a telephone based system and an electronic hand held diary. The second goal of the study is to evaluate a daily diary to evaluate fatigue symptoms in patients with fibromyalgia.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Pfizer Investigational Site, Roseville, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Telephone based system
Electronic Hand Held diary
Time frame: 4 weeks
Time frame: 4 weeks
Time frame: 2 weeks
Time frame: 4 weeks
Time frame: 4 weeks
Looking for future studies?
Notify MePfizer
Industry
A Non-Drug Methodology Study To Explore The Psychometric Properties Of A Daily Diary Of Fatigue Symptoms And To Compare Two Modes Of Administration Of Pain And Sleep Interference Questions For Use With Fibromyalgia Patients
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