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Complementary and Alternative Medicine Sauna Detoxification Study: Phase I

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ClinicalTrials.gov Identifier: NCT01905098
Recruitment Status : Terminated
First Posted : July 23, 2013
Last Update Posted : April 17, 2015
Sponsor:
Collaborators:
National Institutes of Health (NIH)
National Center for Complementary and Integrative Health (NCCIH)
Information provided by (Responsible Party):
Bastyr University

July 16, 2013
July 23, 2013
April 17, 2015
July 2013
September 2013   (Final data collection date for primary outcome measure)
  • Impact of sauna protocol on PCB levels [ Time Frame: 6 weeks ]
    The primary comparison measure will be PCB levels at Sauna Visit 15 in the sauna-first Arm and Observation Visit 4 in the Observation-First Arm.
  • Safety [ Time Frame: 6 weeks ]
    To evaluate the safety of sauna detoxification by recording and describing all adverse events (AE's) throughout the study.
Same as current
Complete list of historical versions of study NCT01905098 on ClinicalTrials.gov Archive Site
Participant-Reported Symptoms [ Time Frame: 6 weeks ]

To describe changes in quality of life and participant-reported symptoms associated with participation in the study.

Query for symptoms will be recorded daily during all sauna visits (SV1-15), at each observation visit (OV1-4), and at the End of Study Visit.

The RAND Short Form 36 Questionnaire, and NIH Patient-Reported Outcomes Measurement Information System (PROMIS) Questionnaires: Global Wellness, Fatigue, Physical Function will be assessed at SV1, OV1, and End of Study Visit.

Same as current
Not Provided
Not Provided
 
Complementary and Alternative Medicine Sauna Detoxification Study: Phase I
Complementary and Alternative Medicine Sauna Detoxification Study: A Phase I Randomized 2-Arm Study to Determine the Impact of Hyperthermia Intervention Protocol on Serum Polychlorinated Biphenyls (PCBs) in Healthy Human Adults.
The purpose of this study is to determine the impact of sauna use on polychlorinated biphenyls (PCB) in the blood of healthy human adults, as well as to assess safety, feasibility, and tolerability, and effects on quality of life and wellness. We hope to determine if there is a link between lower PCB levels in blood and sauna use.

This is a Phase I, 2-Arm randomized trial.

All study participants will actively undergo sauna intervention sessions and observation sessions.

The time between Phone Screen and the End of Study Visit will vary by individual schedule. For the purposes of this study, a participant will be considered 'actively enrolled' when s/he has signed the Full Study Consent Form on the first sauna or observation visit (SV1 or OV1). Each participant will be actively enrolled for at least 7 weeks, but no more than 22 weeks.

All participants will undergo Phone Screen for eligibility prior to participating in any study-related visits. Candidates will first be asked for their oral consent to be screened, and if granted, questioning will continue. If the participant meets pre-screening criteria assessed on the phone, they will be asked to schedule an In-Person Screening Visit.

Prior to randomization, all participants will participate in an In-Person Screening Visit at the Bastyr University (BU) Clinical Research Center (CRC) for: informed consent, to have a blood draw for screening lab analysis, anthropomorphic measurements, a 12-lead ECG assessment, provide demographic data, and medical history assessment.

If participants remain interested and eligible, they will be randomized into either Sauna-First Arm or Observation-First Arm within 2 weeks of eligibility ascertainment using block randomization scheme.

Participants will know that they are in an intervention, but will not know their PCB levels, or the results of questionnaire assessments until approximately three months after the end of the study. The PI will review monitoring and AE data, but will be blinded to PCB data during analysis.

After screening, randomization, and informed consent, study participants in either Arm will either complete a 3-week observation period followed by a 3-week medically monitored sauna-based detoxification intervention; or will first complete a 3-week medically monitored sauna-based detoxification intervention, followed by a 3-week observation period. Each participant will also have an End of Study Visit at least 7 days after the last study visit (Sauna or Observation Visit -depending on the Arm).

The sauna will be pre-warmed to 160 degrees Fahrenheit and humidity set to 25% +/- 5%. Participants will have a scheduled 10-min break every 30 minutes of sauna, during which time vital signs, symptoms, and fluid intake will be assessed and recorded.

During Sauna Visits weekly lab assessments will be performed to compare participants' baseline lab values with those during the sauna intervention, and to monitor for safety. In addition, weekly serum samples will be taken for PCB assessment.

During each Observation Visit a blood draw for Complete Blood Count with Differential (CBC/D), Comprehensive Metabolic Panel (CMP), and PCBs analysis will be performed, as well as query for symptoms and MOSES questionnaire will be assessed.

Interventional
Phase 1
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: None (Open Label)
Hyperthermia
  • Other: Sauna Detoxification Protocol

    All study participants will actively undergo sauna intervention sessions.

    The sauna will be pre-warmed to 160 degrees Fahrenheit and humidity set to 25% +/- 5%. Participants will have a scheduled 10-min break every 30 minutes of sauna, during which time vital signs, symptoms, and fluid intake will be assessed and recorded.

    On a weekly basis, lab assessments will be performed to compare participants' baseline lab values with those during the sauna intervention, and to monitor for safety. In addition, weekly serum samples will be taken for PCB assessment.

    Other Name: Sauna-based detoxification
  • Other: Observation Sessions
    All enrolled participants will undergo observation protocol consisting of one (1) hour visit weekly consistent with Sauna Visits lab assessment time points, to be completed in 3 weeks (4 total sessions within 21 days). At each Observation Visit a blood draw for CBC/D, CMP, and PCBs analysis will be performed, as well as query for symptoms and MOSES questionnaire will be assessed.
  • Experimental: Observation-First Arm

    A group that first attends 4 observation visits without sauna, and then attends sauna sessions 5 times a week for 3.5 hours per visit for 3 weeks.

    Participants in this Arm will undergo both listed interventions: Observation and Sauna Protocols.

    Interventions:
    • Other: Sauna Detoxification Protocol
    • Other: Observation Sessions
  • Active Comparator: Sauna-First Arm

    A group that first attends sauna sessions 5 times a week for 3.5 hours per visit for 3 weeks and then attends 4 observation visits without sauna.

    Participants in this Arm will undergo both listed interventions: Observation and Sauna Protocols.

    Interventions:
    • Other: Sauna Detoxification Protocol
    • Other: Observation Sessions
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
1
40
April 2014
September 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 21-35 years.
  • Body mass index (BMI) 19 to 29.9 kg/m2 at the screening evaluation.
  • Ability to schedule and attend daily visits for the duration of the study.
  • If female, willingness to use barrier contraception (e.g., cervical cap, diaphragm, condom, metal (non- hormone) Intrauterine Device (IUD) throughout the study and take a pregnancy test at screening and weekly during the study.

Exclusion Criteria:

  • Pregnant, or trying to become pregnant in the three months following screening.
  • Current use of any prescribed pharmaceutical medications (including oral contraceptive pills (OCPs) and dietary supplements).
  • Refusal to stop taking self-prescribed dietary supplements and OCPs for the duration of the study.
  • BMI greater than 29.9 kg/m2 or less than 19 kg/m2.
  • Elevated fasting blood sugar (above 125 mg/dL).
  • Abnormal ECG findings of: bradycardia (heart rate below 60) not due to athletic bradycardia, ventricular arrhythmias, axis deviation, coronary circulation problems (ischemia/infarct/injury), or any activation sequence disorders (e.g. Right/Left Bundle Branch Block (RBBB/LBBB) and Wolff-Parkinson-White Syndrome (WPW).)
  • Hyper or hypotension (BP above 180/100 or below 80/50 respectively).
  • A reported diagnosis of any chronic medical condition (e.g., multiple sclerosis, diabetes, or endocrine disorders, liver disease, kidney disease, HIV/AIDS, or cancer), or with a reported history of substance abuse or mental illness within the past 5 years, or a mental health disorder in the past 6 months.
  • CBC/D, ALT-Liver Protein, AST-Liver Protein, Blood Urea Nitrogen (BUN), or Creatinine outside of 15% of the Lower/Upper Limit of Normal (LLN/ULN) values.
  • Recent infection (<14 days), open sores, or communicable skin conditions.
  • Current reported use of any tobacco products or illicit drugs.
  • Any condition that, in the opinion of the investigators or Institutional Review Board (IRB), would preclude the safe completion of the study (e.g., clinical or mental health concerns that arise from the overall screening or medical history assessment).
  • Previous participation in the pilot sauna detoxification study, and/or participation in a detoxification program within the last 6 months of the Phone Screen.
Sexes Eligible for Study: All
21 Years to 35 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01905098
H35B11-Phase1
5R00AT004711-04 ( U.S. NIH Grant/Contract )
Yes
Not Provided
Not Provided
Bastyr University
Bastyr University
  • National Institutes of Health (NIH)
  • National Center for Complementary and Integrative Health (NCCIH)
Principal Investigator: Jason Allen, ND, MPH Bastyr University Research Institute
Bastyr University
April 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP