Passive Body Heating, Sleep and Fibromyalgia
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|ClinicalTrials.gov Identifier: NCT01557062|
Recruitment Status : Completed
First Posted : March 19, 2012
Last Update Posted : March 19, 2012
Objectives: To assess the effect of passive body heating on the sleep pattern of patients with fibromyalgia.
Methods: Six menopausal women diagnosed with fibromyalgia according to criteria determined by the American College of Rheumatology were included. All women underwent passive immersion in a warm bath at 36±1 °C, for 15 sessions of 30 minutes each over 3 weeks. Their sleep pattern was assessed by polysomnography at the following conditions: pre-intervention (baseline), on the first day of intervention (acute), on the last day of intervention (chronic) and 3 weeks after the end of interventions (follow-up). Core body temperature was evaluated by a thermistor pill at the above-mentioned conditions. The impact on fibromyalgia was assessed through of a specific questionnaire called fibromyalgia impact questionnaire.
|Condition or disease||Intervention/treatment||Phase|
|Fibromyalgia||Other: Polysomnography Other: Teperature measure Other: Fibromyalgia Impact questionary||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||25 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Passive Body Heating Improves The Sleep Pattern In Women Patients Fibromyalgia|
|Study Start Date :||March 2009|
|Actual Primary Completion Date :||March 2010|
|Actual Study Completion Date :||December 2010|
The Embla® S7000 was used to record full-night at the Sleep Institute (São Paulo, Brazil). The sensors were attached to the patient in a non-invasive manner using tape or rubber bands. The physiological variables were monitored simultaneously and continuously: 4 channels of EEG, 2 of EOG, 4 of EMG and 1 channel of ECG. Airflow detection was made through 2 channels using a pair of thermal sensors and nasal pressure. Respiratory effort of the chest and abdomen, were measured by respiratory inductance plethysmography. Oxygen saturation, were measured with a pulse oximeter. Sleep stages were visually scored in all the PSG according to standardized criteria for the investigation of sleep macrostructure.
Other: Teperature measure
Core body temperature was assessed using a thermistor pill (sensor), which is an electronic device 2.23 cm in length and 1.06 cm in diameter that records body temperature and transmits it to a receptor located at the patient's waist called the Core Body Temperature Monitoring System (CorTempTM), that is powered by a silver oxide battery. The components of the sensor are encapsulated in epoxy resin and coated with silicone (HQ Inc., Florida, USA). To ensure that the sensor would be in the intestines and not the stomach, the pill was ingested at least 2 hours (h) before beginning temperature recording. The CBT was recorded every 30 minutes (min) between 10:00pm and 7:00am. The time of pill elimination is variable between individuals and may be as long as 48h.
|Fibromyalgia Impact questionary||
Other: Fibromyalgia Impact questionary
The FIQ is an instrument used to assess the quality of life specifically for patients with FM. This questionnaire consists of 19 questions related to functional capacity, employment status, general well being, psychological disorders and physical symptoms. The higher the score is, the greater is the impact of FM in the individual's quality of life. This questionnaire was validated for Brazilian's population in 2006.
- Sleep Pattern [ Time Frame: 7 weeks. Was measured the sleep parameters from: Baseline to acute's time point (at the first day of intervention); Acute to chronic's time point (after 15 sections); Chronic's to follow-up time point (at 15 days after end point of interventions). ]Polysomnographies's register
- Impact of Fibromyalgia Disease [ Time Frame: 7 weeks- The measurements occurred at the following time points: baseline, chronic and follow-up. ]Fibromyalgia Impact Questionnaire (FIQ)
- Changes in Core Body Temperature (CBT) [ Time Frame: 7 weeks. Was measured the CBT from: Baseline to acute's time point (at the first day of intervention); Acute to chronic's time point (after 15 sections); Chronic's to follow-up time point (at 15 days after end point of interventions). ]was monitored continuously throughout the nights at baseline and on days of the experimental protocols by a thermistor pill with a CorTemp HT150002 and core temperature sensor coupled with a data recorder.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01557062
|Federal University of Sao Paulo|
|Sao Paulo, SP, Brazil, 04020-050|
|Principal Investigator:||Marco T De Mello, Ph.D||Federal University of São Paulo|
|Study Chair:||Adressa Silva, MD||Federal University of São Paulo|
|Study Chair:||Sandra S Queiroz||Federal University of São Paulo|
|Study Chair:||Mônica L Andersen, Ph.D||Federal University of São Paulo|
|Study Chair:||Marcos Mônico-Neto||Federal University of São Paulo|
|Study Chair:||Raquel MS Campos, MD||Federal University of São Paulo|
|Study Chair:||Suely Roizenblatt, Ph.D||Federal University of São Paulo|
|Study Chair:||Sergio Tufik, Ph.D||Federal University of São Paulo|