Evaluating Qigong as a Clinical Intervention for Cancer Survivors' Fatigue

Sponsor
The Miriam Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02845492
Collaborator
Brown University (Other)
60
1
2
17
3.5

Study Details

Study Description

Brief Summary

This study compares Qigong movement-based meditation exercise with a healthy living exercise-wellness course. There are two primary goals of this research:

  1. Evaluate and compare physiological mechanisms underlying the two wellness-exercise interventions with the specific goal of understanding the physiology of Qigong.

Using a simple noninvasive EEG setup, the study will test some of the same brain mechanisms that have been found in mindfulness meditation.

The study will also investigate Qigong's effects on stress and heart signals and on inflammation in the immune system. A key hypothesis is that Qigong will show distinctive, stronger effects on brain and heart measures. A related hypothesis is that Qigong will show stronger effects on blood markers of inflammation.

  1. Compare effect sizes of the two interventions in decreasing fatigue in order to plan for a larger clinical trial.
Condition or Disease Intervention/Treatment Phase
  • Other: Qigong
  • Other: Complete Health Improvement Program (CHIP)
N/A

Detailed Description

Between 20-50% of Cancer Survivors report fatigue following treatment that interferes with their daily life. However, to date no treatment option has been definitively validated as effective for fatigue in survivors. In recent years Mind Body exercises such as yoga, Tai Chi, and Qigong have been shown in small clinical trials to be effective at treating the symptoms of CRF in a wide array of Cancer types. But understanding of basic science mechanisms is poor.

Recent studies of Mindfulness meditation, by the investigators and others, confirm the importance of brain mechanisms related to awareness and attention. This study will assess whether Qigong activates similar physiological processes. The study will also assess (1) whether emotion regulation improves, suggesting that Mindfulness-related processes may partially underlie changes in Qigong as a Mindful exercise (2) whether grip strength improves, suggesting that Qigong activates similar processes to conventional exercise.

As an exploratory question, the study will look at whether brain measures related to awareness are correlated with inflammatory markers called cytokines, suggesting possible neuro-immune interaction that may be relevant for understanding fatigue, vitality and embodied meditative movement therapies such as Qigong, Tai Chi and Yoga.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Testing the Effects of Qigong on a Multi-System Neuro-muscular- Immune Model of Vigor in Cancer Survivorship
Study Start Date :
Jul 1, 2016
Anticipated Primary Completion Date :
Apr 1, 2017
Anticipated Study Completion Date :
Dec 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Qigong intervention

Qigong meditative exercise intervention meets three times a week for 10 weeks. The qigong group (n=30) will meet at the Women's Medicine Collaborative, Miriam Hospital (146 W. River St., Providence, RI) for Qigong classes. The lesson will be taught by a validated Qi Gong master with over forty years of experience and the interventional protocol will be validated. Two and a half hours of weekly outside personal practice will also be required of participants.

Other: Qigong
Qigong is a mind-body exercise based around gentle exercise and the cultivation of a meditative focus on bodily sensations
Other Names:
  • Meditative Exercise Therapy
  • Active Comparator: CHIP healthy wellness-exercise class

    The Complete Health Improvement Program is a validated set of weekly classes designed to promote gentle exercise and wellness related activities in a supportive group setting led by an experienced trainer.

    Other: Complete Health Improvement Program (CHIP)
    The CHIP program is a validated weekly wellness and exercise program designed to promote health and wellbeing.
    Other Names:
  • Wellness-Exercise Program
  • Outcome Measures

    Primary Outcome Measures

    1. Fatigue Symptom Inventory Questionnaire [Change from baseline to 10 weeks]

      Questions about daily experience of fatigue

    Secondary Outcome Measures

    1. EEG meditative brain measures, [at baseline and at 10 weeks]

      Acquired using a non-invasive EEG cap that sits on the scalp

    2. Self-reported Vitality (a component of the Medical Outcomes Short-Form 36) [at baseline and 10 weeks]

    3. Heart Rate Variability (HRV) [at baseline and 10 weeks]

      Acquired using an EKG

    4. Inflammatory cytokines [at baseline and 10 weeks]

      Cytokine measures: Il-1, Il-6, Il-10, tnf-alpha

    Other Outcome Measures

    1. Difficulties in emotion regulation self-report scale (DERS) [at baseline and 10 weeks]

      Questions about emotions and emotion regulation

    2. Handgrip strength [at baseline and 10 weeks]

      Uses dynamometer to assess handgrip strength

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Female patients

    • Aged 18-70 years

    • Self-report of fatigue =/> 3/10 on fatigue interference scale

    • Have been diagnosed and completed treatment for cancer (with surgery or radiation or chemotherapy)

    • no surgery, radiation or chemotherapy received in the past 8 weeks (ongoing treatment with Herceptin [trastuzumab] or other adjuvant therapies is permitted)

    • Currently cancer-free

    • Have a primary care or other physician

    • Ability to understand English

    • Willingness to have blood drawn, have an EEG taken and complete questionnaires

    • Ability to pass basic validated physical movement tests (e.g.: standing with feet touching for 30 seconds, twist right to left and back, hold arms out to side in air for 15 seconds, lift arms over head, moving from standing position to seated position on the floor) to verify safety for Qigong practice.

    Exclusion Criteria:
    • History or current diagnosis of medical or psychiatric disorder that would interfere with ability to participate in wellness classes or in scientific assessment sessions (e.g., rheumatoid arthritis, diabetes, major psychiatric disorder, connective tissue disorder)

    • Body Mass Index (BMI) > 31

    • Active alcohol or drug abuse

    • Tobacco use

    • Pregnancy

    • Regular daily use of anti-inflammatory drugs, including non-steroidal anti-inflammatory drugs, (does not apply to common use of daily "baby aspirin" as daily prophylactic cardiovascular treatment)

    • Resting systolic blood pressure of less than 90 or greater than 160 and resting diastolic blood pressure of greater than 110.

    • Ingestion of caffeine or cocoa products less than two hours from data collection

    • Contraindication to regular physical activity participation

    • Already engaging in >60 min of vigorous physical activity per week for the prior month

    • Weekly practice of yoga, Tai Chi, Qigong, or meditation since the diagnosis of cancer

    • Peripheral neuropathy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Miriam Hospital Providence Rhode Island United States 02904

    Sponsors and Collaborators

    • The Miriam Hospital
    • Brown University

    Investigators

    • Principal Investigator: Catherine Kerr, PhD, Women's Medicine Collaborative, Miriam Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Catherine Kerr, Assistant Professor of Family Medicine, The Miriam Hospital
    ClinicalTrials.gov Identifier:
    NCT02845492
    Other Study ID Numbers:
    • MiriamH
    First Posted:
    Jul 27, 2016
    Last Update Posted:
    Aug 1, 2016
    Last Verified:
    Jul 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by Catherine Kerr, Assistant Professor of Family Medicine, The Miriam Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 1, 2016