The Effectiveness of Oral Health Promotion on Pneumonia Complicating Stroke

Sponsor
Anhui Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT04095780
Collaborator
(none)
166
1
2
31
5.4

Study Details

Study Description

Brief Summary

To investigate the evidence for the integration of oral health promotion as part of interdisciplinary stroke rehabilitation.

Condition or Disease Intervention/Treatment Phase
  • Other: Advanced oral hygiene care programme
  • Other: Oral hygiene instruction
N/A

Detailed Description

Pneumonia complicating stroke is very difficult to manage and has a very poor prognosis, leading to a significantly higher risk of death. Oral opportunistic pathogens have been reported to be associated with the incidence of pneumonia among non-stroke immunocompromised subjects. Preliminary studies found that patients with stroke had higher carriage rates of oral opportunistic pathogens than healthy subjects. Therefore, investigators hypothesize that pneumonia complicating stroke is associated with oral opportunistic pathogens, and oral health promotion interventions may reduce the incidence of pneumonia complicating stroke via its effects on the species and relative abundance of oral opportunistic pathogens. In order to prove this, investigators need to (1) firstly conduct a randomized controlled trial to confirm whether oral health promotion is able to reduce the levels of plaque, and the incidence of pneumonia complicating stroke at clinical level; (2) secondly employ metagenomics analysis to compare oral rinse samples and respiratory samples, and to identify pneumonia-associated "oral opportunistic pathogens group"; (3) finally elucidate how oral health promotion influences the species and relative abundance of oral opportunistic pathogens. This proposed study will provide evidence for the integration of oral health promotion as part of interdisciplinary stroke rehabilitation.

Study Design

Study Type:
Interventional
Actual Enrollment :
166 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness of Oral Health Promotion on Pneumonia Complicating Stroke
Actual Study Start Date :
Nov 1, 2018
Actual Primary Completion Date :
Jun 1, 2021
Actual Study Completion Date :
Jun 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Advanced oral hygiene care programme

Patients with stroke will receive the advanced oral hygiene care programme (AOHCP) comprising powered tooth brushing and mouth rinsing with chlorhexidine (with a supply of standardized power tooth brushes, mouth rinse, tooth paste and oral hygiene instruction).

Other: Advanced oral hygiene care programme
Brush teeth with standardized power tooth brush twice a day. Rinse mouth with chlorhexidine twice a day. Oral hygiene education

Experimental: Oral hygiene instruction

Patients with stroke will only receive the oral hygiene instruction.

Other: Oral hygiene instruction
Oral hygiene education

Outcome Measures

Primary Outcome Measures

  1. The prevalence of pneumonia complicating stroke [1 week]

    To calculate and compare the incidence of pneumonia between interventional group and control group, to identify whether the intervention approach could reduce the short-term incidence after the baseline.

Secondary Outcome Measures

  1. The prevalence of pneumonia complicating stroke [1 month, 3 months, 6 months]

    To calculate and compare the long-term incidence of pneumonia between interventional group and control group.

  2. Metagenomic [3 days, 5 days, 7 days, and 1 month, 3 months, 6 months]

    To analyze composition and relative abundance of oral microbiome in oral rinse samples.

  3. Plaque Index [1 month, 3 months, 6 months]

    0 = no plaque detected with probe; 1 = plaque not visible by unaided eye but detectable with probe; 2 = moderate amount of plaque; 3 = abundance of plaque

  4. Gingival Bleeding Index [1 month, 3 months, 6 months]

    0 = no bleeding after probing; 1 = presence of bleeding within 10 seconds after probing.

  5. the Short Form Health Survey 12 (SF-12) [1 month, 3 months, 6 months]

    The SF-12 consists of 12 items covering eight conceptual domains of health: general health (GH), physical functioning (PF), bodily pain (BP), role-physical (RP), mental health (MH), vitality (VT), social functioning (SF), and role-emotional (RE). Four items are reversed for scoring (item no.: 1, 8, 9, and 10). The SF-12 consists of 12 items and each of them has its own physical component summary (PCS) and mental component summary (MCS) regression coefficients. The response to each item will be multiplied by its PCS regression coefficient and added together with the PCS constant to provide Physical Health summary scores (SF-12 PCS). Mental Health summary scores (SF-12 MCS) will be calculated likewise. A higher scores mean a better outcome.

  6. the Oral Health Impact Profile 14 (OHIP-14) [1 month, 3 months, 6 months]

    0=never, 1=hardly ever, 2=occasionally, 3=fairly often, and 4=very often/all of the time. Summary OHIP-14 score and domain scores will be derived by summating responses to each item (i.e. score 2, 3, and 4). A higher scores mean a worse outcome.

  7. the Geriatric Oral Health Assessment Index (GOHAI) [1 month, 3 months, 6 months]

    1 = always, 2 = often, 3 = sometimes, 4 = seldom, and 5= never. Summary GOHAI scores will be derived by summating responses to items after reversing the coding of the three positively worded items (swallowing, appearance, and discomfort when eating). A higher scores mean a better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • having onset of stroke within 3 days and free of any post-stroke complication

  • having moderate to severe functional disability- Barthel Index (BI) scores of <70

  • being conscious and respiring voluntarily without ventilator

  • not having any lung disease and lower respiratory infection

  • not have an indwelling naso-gastric feeding tubes

  • having dysphagia as showed by GUSS test (The Gugging Swallowing Screen, GUSS)

  • having normal cognitive ability or mild impairment- Mini Mental State Examination (MMSE) >18

  • having ability to follow instruction (as an assessment of compliance of oral health intervention)

  • not having systemic administration of antibiotics

  • not being edentulous

Exclusion Criteria:
  • mild disability (Barthel Index > 70)

  • having normal swallowing function

  • edentulous

  • having an indwelling naso-gastric feeding tubes

  • having communication disorders, unable to cooperate with family caregivers for oral health promotion

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Second People's Hospital of Hefei Hefei Anhui China 230000

Sponsors and Collaborators

  • Anhui Medical University

Investigators

  • Study Director: Ruoxi Dai, PhD, Lecturer

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ya Zhang, Principal Investigator, Anhui Medical University
ClinicalTrials.gov Identifier:
NCT04095780
Other Study ID Numbers:
  • 81701036
First Posted:
Sep 19, 2019
Last Update Posted:
Jul 21, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ya Zhang, Principal Investigator, Anhui Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 21, 2022