Clinical Trial: Meditation and Stretching for Post Treatment Lyme Disease Syndrome

Study Status: Completed
Recruit Status: Unknown status
Study Type: Interventional

Official Title: Meditation and Stretching for Post Treatment Lyme Disease Syndrome

Brief Summary: The investigators wish to conduct a preliminary study to examine the efficacy of meditation among patients with Post Treatment Lyme Syndrome (PTLDS). Specifically, the investigators will use the breathing, meditation, and stretching techniques common to Kundalini Yoga practice. The investigators plan to assess the degree in which this practice can reduce Post-Treatment Lyme Disease symptoms. Because fatigue and pain are so common among patients with PTLDS, the primary focus of this study will be fatigue and pain. Secondary outcomes will include cognitive complaints, physical and mental functioning, medical utilization, somatic symptoms, and psychopathology.

Detailed Summary:

The CDC reports that approximately 10-20% of patients treated for Lyme disease with the IDSA-recommended 2-4 week course of antibiotics will continue to have symptoms of fatigue, pain, or joint and muscle aches despite prior antibiotic treatment. The symptoms can last months or even years after treatment. The medical community officially calls this condition "Post-treatment Lyme disease Syndrome" (PTLDS) but some have called it "chronic Lyme disease." Because some patients with PTLDS continue to have ongoing symptoms despite many additional courses of antibiotics beyond the standard course, alternative non-antibiotic treatment programs need to be explored. The proposed study seeks to evaluate the efficacy of meditation among those patients that have been previously treated for Lyme disease but are still continuing to experience prominent symptoms of fatigue and/or pain.

During this study, patients will be screened initially over the telephone to assess eligibility, sign consent with the study treating psychiatrist, and complete self-report questionnaires. Forty patients will be enrolled. Of these, 20 will be randomly assigned to meditation group therapy and 20 will be assigned to a wait-list. Assessments will be conducted prior to treatment, at 4 weeks and at 8 weeks. There will also be a 6 month follow-up by questionnaire and telephone interview. Study participants randomized to the wait-list control group will then be offered, after 8 weeks, the option of joining a meditation group for 8 weeks. Each meditation group will be composed of 6-8 subjects.

Should this study find evidence suggesting that meditation therapy is helpful in reducing the symptoms of PTLDS, this would be a valuable finding that would lead to a larger study as it has important public health implications for many individuals now quit
Sponsor: Research Foundation for Mental Hygiene, Inc.

Current Primary Outcome:

  • Fatigue (Self-reported changes in the levels of fatigue as measured by the PROMIS Fatigue Scale) [ Time Frame: 8 weeks ]
    Self-reported changes in the levels of fatigue as measured by the PROMIS Fatigue Scale
  • Pain (Self-reported changes in the levels of pain as measured by the PROMIS Pain Interference Scale) [ Time Frame: 8 weeks ]
    Self-reported changes in the levels of pain as measured by the PROMIS Pain Interference Scale
  • Global Health (Self-reported changes in the levels of satisfaction with global health as measured by the PROMIS Global Heath Satisfaction Scale) [ Time Frame: 8 weeks ]
    Self-reported changes in the levels of satisfaction with global health as measured by the PROMIS Global Heath Satisfaction Scale


Original Primary Outcome: Same as current

Current Secondary Outcome:

  • Physical & Social Functioning (Self-reported changes in the levels of satisfaction with physical and social functioning as measured by the PROMIS Physical Functioning Scale & Social Satisfaction Scale) [ Time Frame: 8 weeks ]
    Self-reported changes in the levels of satisfaction with physical and social functioning as measured by the PROMIS Physical Functioning Scale & Social Satisfaction Scale
  • Multisystemic Symptoms (Self-reported changes in symptom severity as indicated in the Multisystem Symptom Questionnaire) [ Time Frame: 8 weeks ]
    Self-reported changes in symptom severity as indicated in the Multisystem Symptom Questionnaire
  • Mood (Anxiety and/or Depression) (as measured by the Beck Depression Inventory, PROMIS Depression & Anxiety Scales) [ Time Frame: 8 weeks ]
    Self reported changes in mood as measured by the Beck Depression Inventory, PROMIS Depression & Anxiety Scales
  • Acceptance of Treatment (as indicated by the patient log) [ Time Frame: 8 weeks ]
    Self reported time spent on practicing meditation across 8 weeks as indicated by the patient log.
  • Medical Utilization [ Time Frame: 6 month after treatment completion ]
    Assess medical utililization during the 3 month interval prior to treatment and prior to 6 month follow-up


Original Secondary Outcome: Same as current

Information By: Research Foundation for Mental Hygiene, Inc.

Dates:
Date Received: January 16, 2015
Date Started: January 2015
Date Completion:
Last Updated: January 26, 2015
Last Verified: January 2015