Effect on Parkinson's Disease After Therapeutic Induction of CranioSacral Integrated Therapy
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: biweekly intervention.
- Who it may be relevant to
- Registry conditions: Parkinson's Disease. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
We are studying \& researching the effect of CranioSacral Integrative therapy on Parkinson's Diseased Patients for 3 months. With a therapeutic induction via manual CranioSacral integrative therapy for 90 minutes per session with a total of 2 session divided equally in a month (biweekly intervention). At the end of 3 months each patient will have total of 9 hours of CranioSacral Integrative therapy induced, we will document the symptoms and shortcomings of the patients at evaluation, before and after therapeutic treatment on a measured scale ranging from 1-10. Finally graphically and statistically measure the quality of change in the symptoms at the end of 3 months and provide executive summary of the research finding, which the investigators expect to be a positive one.
Detailed description
We are studying \& researching the effect of CranioSacral I therapy on Parkinson's Disease
Interventions
- Other biweekly intervention
10 step craniosacral therapy protocol through manual therapy at feet , thoracic diaphragm, neck and cranium
Primary outcome measures
- reduction in tremors due to Parkinson's disease in the patient [Time frame: 3 months]
Secondary outcome measures (1)
- Quality of Proprioception [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- must be Diagnosed with Parkinson's Disease
Exclusion criteria
- Anyone without Parkinson's Disease
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
United States · 1 center
- Naturalmed therapy — Ann Arbor
Identifiers
NCT: NCT01989013 · CST001