This study will compare subjects with a history of pelvic or menstrual pain diagnosed with endometriosis treated at Clear Passage with untreated control subjects. The treatment group will be a retrospective chart review; the control subject group will be a prospective questionnaire based study. The study will assess the changes in pain experienced by subjects treated with manual therapy at Clear Passage to untreated subjects with endometriosis.
This study has two segments the first is a chart and outcome assessment of patients treated at Clear Passage (CP) with a diagnosis of endometriosis. These patients have completed multiple questionnaires as a standard of care for outcome monitoring in the clinic setting, no new data will be collected. The second segment is a prospective observational, online questionnaire based study of female subjects with a diagnosis of endometriosis not treated at CP. Data on the impact of quality of life (QOL) over time of subjects not treated at CP will be assessed using the same questionnaire used as standard of care in the clinic twice, 30 days apart. This will be accomplished using online forms with subjects able to complete the questionnaires with ease via the internet. The data obtained from the untreated subjects will allow for reporting of overall impact on QOL in this population, as well as provide a control group for assessment of improvement for manual therapy interventions for patients with endometriosis.
Study Type
OBSERVATIONAL
Enrollment
8
Manual Physical Therapy intervention using the Clear Passage Approach (CPA). The focus of the CPA is to deform adhesions throughout the body using a variety of manual therapy techniques and modalities.
Clear Passage Physical Therapy
Gainesville, Florida, United States
Reported overall pain rating
Self reported values using the Pain Questionnaire
Time frame: 30 days
Reported Global Health
Self reported values using the Global Health Questionnaire
Time frame: 30 days
Reported Pain Intensity
Self reported values using the Pain Interference Questionnaire
Time frame: 30 days
Reported Sexual Function
Self reported values using the Female Sexual Function Index Questionnaire
Time frame: 30 days
Correlations to positive treatment outcomes
Medical history correlations for positive outcomes in subjects treated with manual therapy
Time frame: 30 days
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