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Efficacy of Passive Oral Motor Therapy on Drooling in Children With Multiple Disabilities

Primary Purpose

Multiple Disabilities

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
passive oral motor therapy for drooling
Sponsored by
Maharishi Markendeswar University (Deemed to be University)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Disabilities

Eligibility Criteria

7 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children aged 7-19 yrs (male and female)
  • Confirmed diagnosis of multiple disability Score of ≤ 3 on drooling severity and frequency scale (indicating moderate to profuse drooling)
  • Medication, taken to treat drooling, stopped at least 3 months before start of the study

Exclusion Criteria:

  • No History of Previous surgical procedure for saliva control
  • Use of drugs that interfere with saliva secretion (anticholinergic and neuroleptic drugs, benzodiazepines)
  • Use of oral prosthetic devices
  • Tactile hypersensitivity and oral problems like caries, toothache
  • Congenital defects like cleft palate
  • systemic diseases (bronchial asthma, congenital heart failure, and myasthenia gravis)
  • Previous surgical procedures in the oral/nasal cavity interfering with saliva production
  • Respiratory dysfunction

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Passive oral motor therapy group

    Arm Description

    All the subjects received passive treatment which included light touch, stroking, vibration, tapping, pressure and stretch. All the techniques have been proved to be effective in treating drooling. Relative sterility and hygiene was maintained throughout the procedure as sterilized gloves and napkins were used. The measurement protocol was designed to check effectiveness on drooling in children. The protocol was given for 4 weeks with treatment sessions given 3 times per week and the treatment duration was 30min.12 sessions of oral motor stimulation therapy given during the 4 weeks..

    Outcomes

    Primary Outcome Measures

    Drooling Frequency and Severity rating scale

    Secondary Outcome Measures

    Drool Quotient method
    METHOD OF ASSESSMENT OF SEVERITY OF DROOLING

    Full Information

    First Posted
    January 1, 2015
    Last Updated
    January 7, 2015
    Sponsor
    Maharishi Markendeswar University (Deemed to be University)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02333981
    Brief Title
    Efficacy of Passive Oral Motor Therapy on Drooling in Children With Multiple Disabilities
    Official Title
    Efficacy of Passive Oral Motor Therapy on Drooling in Children With Multiple Disabilities
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    August 2012 (undefined)
    Primary Completion Date
    December 2012 (Actual)
    Study Completion Date
    May 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Maharishi Markendeswar University (Deemed to be University)

    4. Oversight

    5. Study Description

    Brief Summary
    This study was formulated to determine the efficacy of passive oral motor regimen for drooling in children with multiple disabilities. Seven subjects aged 7-19yrs were taken in the study. All the subjects received passive treatment which included light touch, stroking, vibration, tapping, pressure and stretch. All the techniques have been proved to be effective in treating drooling. Relative sterility and hygiene was maintained throughout the procedure as sterilized gloves and napkins were used. The measurement protocol was designed to check effectiveness on drooling in children. The protocol was given for 4 weeks with treatment sessions given 3 times per week and the treatment duration was 30min. Twelve sessions of oral motor stimulation therapy given during the 4 weeks. Thirteen after 4 weeks of treatment, improvement was found in terms of the severity as well. Primary outcome measure taken was Drooling Frequency and Severity rating scale and secondary outcome measure being taken was drool quotient. Pre and post intervention scores of Drooling Frequency and Severity rating scale and drool quotient were taken and data was analyzed using wilcoxon signed rank test .
    Detailed Description
    Title To formulate and see efficacy of passive oral motor regimen for drooling in children with multiple disabilities Background Drooling ranges from mild embarrassment and discomfort for the intellectually intact patient with minimal drooling to gross emotional and physical impairment for the severely affected individual. Drooling produces an unhygienic condition that may be associated with a disagreeable odour. Drooling affects the social and physical wellbeing of children and may represent problems for caregivers. Many persons with severe and profound disabilities exhibit chronic and excessive drooling, which can have unfavourable effects on their socialization and health. Studies have suggested that various treatments like medication, surgery, behaviour modification, myofunctional therapy and oral motor therapy are effective in treating drooling but there is no single protocol developed to treat drooling in children with multiple disabilities. Passive treatment protocol is needed specifically designed for children who are not able to follow commands and on whom various treatment techniques like behaviour modification, over-correction can't be applied. Present study aims to formulate and see the efficacy of passive oral motor regimen for drooling in children with multiple disabilities. Methodology Seven subjects of age group between 07-19 years were selected out of accessible population. Informed consent taken from the parents/caregivers.Severity and frequency of drooling accessed (For each subject prior to the study) and Drool Quotient was calculated (For each subject prior to the study). Patient was in sitting position with back fully supported and head in neutral position in their own home. Therapist in standing position in front of the patient.Therapist wore sterilised gloves to ensure that no infection occurs along with change of gloves for every subject. Light touch applied to mid line of lips (3 times, for 5 sec). Maintained pressure applied around lips (3 times for 3 sec). Gentle tapping to the cheeks applied with index finger (8 times each cheek). Quick, gentle stretch applied outward with index and middle finger on middle of upper lip and lower lip (8 times on each lip). Gentle stroke to the cheek applied with index finger from base of nose towards ear. Then returned back to corner of lips (8 times each cheek), repeat on the other side. Gentle stroking applied to area around the lips in a circular manner, from the corner towards the center and to the other corner, then reverse. (4 times each lip). Vibration slowly applied for 10-15 sec each of a) orbicularis oris b) Both sides of larynx from chin to sternal notch c) Under the chin from ear to ear.Quick stretch applied to the masseter muscles (3 times on each side). Stretch pressure applied to vibrated areas, on a) orbicularis oris b) Laryngopharyngeal muscles, both sides. Intra-orally applied light touch to roof of mouth, anteriorly for 3 times. The protocol was given for 4 weeks with treatment sessions given 3 times per week. .

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Multiple Disabilities

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    7 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Passive oral motor therapy group
    Arm Type
    Experimental
    Arm Description
    All the subjects received passive treatment which included light touch, stroking, vibration, tapping, pressure and stretch. All the techniques have been proved to be effective in treating drooling. Relative sterility and hygiene was maintained throughout the procedure as sterilized gloves and napkins were used. The measurement protocol was designed to check effectiveness on drooling in children. The protocol was given for 4 weeks with treatment sessions given 3 times per week and the treatment duration was 30min.12 sessions of oral motor stimulation therapy given during the 4 weeks..
    Intervention Type
    Device
    Intervention Name(s)
    passive oral motor therapy for drooling
    Intervention Description
    7 subjects aged 7-19 yrs were taken . All subjects received passive treatment which included light touch, stroking, vibration with (mechanical vibrator), tapping, pressure and stretch. All the techniques have been proved to be effective in treating drooling. Relative sterility and hygiene was maintained throughout the procedure as sterilized gloves and napkins were used. The measurement protocol was designed to check effectiveness on drooling in children. The protocol was given for 4 weeks with treatment sessions given 3 times per week and the treatment duration was 30min.12 sessions of oral motor stimulation therapy given during the 4 weeks..
    Primary Outcome Measure Information:
    Title
    Drooling Frequency and Severity rating scale
    Time Frame
    4 weeks
    Secondary Outcome Measure Information:
    Title
    Drool Quotient method
    Description
    METHOD OF ASSESSMENT OF SEVERITY OF DROOLING
    Time Frame
    4 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    7 Years
    Maximum Age & Unit of Time
    19 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Children aged 7-19 yrs (male and female) Confirmed diagnosis of multiple disability Score of ≤ 3 on drooling severity and frequency scale (indicating moderate to profuse drooling) Medication, taken to treat drooling, stopped at least 3 months before start of the study Exclusion Criteria: No History of Previous surgical procedure for saliva control Use of drugs that interfere with saliva secretion (anticholinergic and neuroleptic drugs, benzodiazepines) Use of oral prosthetic devices Tactile hypersensitivity and oral problems like caries, toothache Congenital defects like cleft palate systemic diseases (bronchial asthma, congenital heart failure, and myasthenia gravis) Previous surgical procedures in the oral/nasal cavity interfering with saliva production Respiratory dysfunction
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    DIVYA MIDHA, MPT(NEURO)
    Organizational Affiliation
    MAHARISHI MARKANDESHWAR UNIVERSITY
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Efficacy of Passive Oral Motor Therapy on Drooling in Children With Multiple Disabilities

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