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Effects of Osteopathic Visceral Manipulation on the Autonomic Nervous System, Balance and Gastrointestinal Disturbances in Individuals With Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Intervention Protocol
Sham Protocol
Sponsored by
Instituto Docusse de Osteopatia e Terapia Manual
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of Parkinson's;
  • Not having cardiorespiratory diseases;
  • Not being a smoker;
  • Do not use alcoholic beverages;
  • No cognitive deficit;
  • No osteoarticular deformities, plantar ulcers, total or partial amputation of the feet;
  • They do not need auxiliary devices for walking

Exclusion Criteria:

  • Data from individuals with a series of heart rate intervals with less than 95% of sinus beats will be excluded from the study.

Sites / Locations

  • Anne Kastelianne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Intervention Protocol

Sham Protocol

Arm Description

Visceral osteopathic techniques

Simulated visceral osteopathic techniques

Outcomes

Primary Outcome Measures

Change in heart rate variability
For the analysis, frequency domain indices (LF, HF, LF/HF), time domain (SDNN, RMSSD) and geometric indices will be used

Secondary Outcome Measures

Change in balance
For balance analysis we will use the Berg balance scale, validated for the Brazilian population. The overall score is 56 points. A score from 0 to 20 represents impairment of balance, 21 to 40 is acceptable balance, and 41-56 is good balance.
Change in plantar pressure
The static plantar pressure profile will be obtained through pressure sensors present in the platform

Full Information

First Posted
September 3, 2021
Last Updated
September 27, 2021
Sponsor
Instituto Docusse de Osteopatia e Terapia Manual
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1. Study Identification

Unique Protocol Identification Number
NCT05047796
Brief Title
Effects of Osteopathic Visceral Manipulation on the Autonomic Nervous System, Balance and Gastrointestinal Disturbances in Individuals With Parkinson's Disease
Official Title
Effects of Osteopathic Visceral Manipulation on the Autonomic Nervous System, Balance and Gastrointestinal Disturbances in Individuals With Parkinson's Disease: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2021 (Actual)
Primary Completion Date
October 5, 2021 (Anticipated)
Study Completion Date
October 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto Docusse de Osteopatia e Terapia Manual

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction: Parkinson's disease (PD) is responsible for several changes in the body, such as balance, gastrointestinal and autonomic disorders and are associated with impairments in the clinical prognosis of these individuals. In this sense, therapies capable of minimizing this impact are extremely important. Osteopathy has become an alternative treatment for individuals with neurological disorders and has been shown to be effective in treating various conditions, including PD. Objective: a) to evaluate the acute effect of visceral manipulation directed to the intestines and visceral plexuses in the autonomic nervous system of PD patients; b) identify the effect of this approach, after four visits, on balance, plantar pressure, gastrointestinal disorders and autonomic nervous system in this population. Materials and Methods: For this randomized clinical trial, 28 adults diagnosed with PD will be recruited. Subjects will be randomized to protocols in two groups: intervention protocol and placebo protocol, where both will consist of 4 visits twice a week. The intervention protocol will consist of osteopathic manipulative techniques and the sham protocol will consist of simulation of therapy, where the therapist will place his hands in the same regions of the intervention protocol, with superficial contact and without therapeutic intention in each region. The outcome measures of the study will consist of Berg balance assessment and plantar pressure, Rome survey on gastrointestinal disorders, and assessment of autonomic modulation by means of heart rate variability analysis. Volunteers and evaluators will be blind to the protocol and not informed of their order. Only the person responsible for the intervention will not be blind to the protocol. Data will be analyzed according to normality (Shapiro-Wilk test), and comparisons of outcomes between the moments (pre and post) will be performed using the T-student test for paired data or Wilcoxon, as normal and for comparisons between protocols. placebo and intervention, Student's T-test for unpaired data or Mann-Whitney test according to normality will be applied. The adopted statistical significance will be fixed at 5%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Each participant will be randomly assigned to the intervention group or placebo group by an independent study evaluator. Data will be secretly allocated through sealed, opaque envelopes. After the randomization process, the participant will be evaluated by a researcher who will not have knowledge about the distribution of the groups.
Allocation
Randomized
Enrollment
14 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Protocol
Arm Type
Experimental
Arm Description
Visceral osteopathic techniques
Arm Title
Sham Protocol
Arm Type
Sham Comparator
Arm Description
Simulated visceral osteopathic techniques
Intervention Type
Other
Intervention Name(s)
Intervention Protocol
Intervention Description
The intervention protocol will consist of visceral osteopathic techniques and will be performed by a professional who has 17 years of clinical experience in the field of Osteopathy.
Intervention Type
Other
Intervention Name(s)
Sham Protocol
Intervention Description
The sham protocol will be performed by a professional who has 17 years of clinical experience in the field of Osteopathy. The sham protocol will consist of simulation of therapy, where the therapist will place his hands in the same regions of the intervention protocol, without therapeutic intent
Primary Outcome Measure Information:
Title
Change in heart rate variability
Description
For the analysis, frequency domain indices (LF, HF, LF/HF), time domain (SDNN, RMSSD) and geometric indices will be used
Time Frame
T0= before the protocol (15 minutes); T1= until 48 hours after the end protocol (15 minutes)
Secondary Outcome Measure Information:
Title
Change in balance
Description
For balance analysis we will use the Berg balance scale, validated for the Brazilian population. The overall score is 56 points. A score from 0 to 20 represents impairment of balance, 21 to 40 is acceptable balance, and 41-56 is good balance.
Time Frame
T0= before the protocol; T1= until 48 hours after the end protocol
Title
Change in plantar pressure
Description
The static plantar pressure profile will be obtained through pressure sensors present in the platform
Time Frame
T0= before the protocol; T1= until 48 hours after the end protocol

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of Parkinson's; Not having cardiorespiratory diseases; Not being a smoker; Do not use alcoholic beverages; No cognitive deficit; No osteoarticular deformities, plantar ulcers, total or partial amputation of the feet; They do not need auxiliary devices for walking Exclusion Criteria: Data from individuals with a series of heart rate intervals with less than 95% of sinus beats will be excluded from the study.
Facility Information:
Facility Name
Anne Kastelianne
City
Presidente Prudente
State/Province
São Paulo
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data will be shared for any researcher that requests the data by electronic address
IPD Sharing Time Frame
After one year of publication
IPD Sharing Access Criteria
To receive the data, the researcher must have sent a request to nupi@idot.com.br

Learn more about this trial

Effects of Osteopathic Visceral Manipulation on the Autonomic Nervous System, Balance and Gastrointestinal Disturbances in Individuals With Parkinson's Disease

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