Primary Healthcare Center Gulshan-e-Sikandarabad Shireen Jinnah Colony
Karachi, Pakistan
Location contact
Sidra Mohiuddin, MDS
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06356402
This pilot study evaluates the feasibility of conducting a larger Randomized Controlled Trial to compare three oral health education delivery methods to a control group. Except for the control group, mothers in the three intervention groups will receive the same oral health education based on the OHEM module but differ in the delivery methods, namely lecture, exhibition, and demonstration. All groups will receive a booklet and oral hygiene kits and be instructed to educate their children at home. Pre- and post-intervention assessments include the satisfaction of participants, the researchers' evaluation and cost of the trial, oral hygiene status, and the knowledge of the parents and children.
Trial opening soon.
Get Notified12 year–40 year
All sexes
Interventional
Not applicable
Karachi, Pakistan
Sidra Mohiuddin, MDS
PRINCIPAL_INVESTIGATOR
Research question:
There is lacking evidence that oral health education via family-based intervention is effective in improving oral hygiene in children.
OHEM:
A manual, the Oral Health Educational Module (OHEM), has been developed for oral health educators planning a family-based intervention to improve oral health in children by educating and empowering the mothers. OHEM aims to educate mothers about oral health and guide them to share the knowledge with their children. The content includes basic oral health knowledge and the description for preparing and delivering intervention and comes with instruments for assessing the understanding of mothers and children. Educators can choose to carry out the intervention using OHEM via three delivery methods either in a lecture, exhibition, and/or demonstration and each will present the same educational messages.
Objectives:
General objective: To investigate the feasibility of conducting a larger RCT for comparing the efficacy of the OHEM module delivered via lecture, exhibition, and demonstration to a control group.
Primary objective:
Secondary objectives are:
Methods:
Study design: This is a randomized controlled trial feasibility study comparing four groups: Lecture, Exhibition, Demonstration, and Control.
Study location: Ziauddin University Primary Health Care Center, Union Council Gulshan-e-Sikandarabad Kemari, Karachi, Pakistan. The area of Gulshan-e-Sikandarabad comprises five housing blocks.
Sample: The study participants will include mother-child dyads; the intervention is provided to the mothers and the outcomes will be assessed in the mothers and children.
Sample size: The main study assumed that children in the intervention groups would have 6.6 times greater odds of improving their gingival status one level better than before the intervention compared to the control group. Using the Open Epi sample size calculator, the sample size needed for assessing the efficacy of OHEM is n = 112 per group based on 80 % power and 5% significant level and n = 135 per group after accounting for a 20% loss to follow-up (N= 540). The present feasibility study will recruit 30% of the sample which is 41 dyad pairs per group or 164 dyad pairs in four groups.
Sampling technique: A stratified randomized sampling method to select the participants. It will randomly select, i) four of five residential blocks, and then ii) five streets from each block. Each block will be randomly assigned to one of the intervention or control groups.
The systematic random sampling technique (every second household) will be used to select a household with a mother-child dyad from each street.
Data collection:
The control group will receive only the booklet without any instruction and an oral hygiene kit. The participants will be asked not to share the details of the intervention with other participants or individuals known to be involved in the study.
Only one examiner (dentist) will carry out the clinical and behavioral assessments and will be blinded to the intervention group assignment.
Instrument and tools The following tools will be used to collect the data from the mother-child dyad.
i. Feasibility assessment measures:
ii. Dental plaque index using Silness and Loe criteria at pre- and post-intervention
iii. Gingival index using Loe and Silness criteria at pre- and post-intervention
iii. OHEM-KAP (Knowledge, attitude, practices) Questionnaire for mothers and children at pre- and post-intervention
iv. Tooth brushing and Dental flossing skills checklist at pre- and post-intervention
v. OHIP-14 (Oral health impact profile - 14) Questionnaire at pre- and post-intervention
Intervention The intervention will deliver the same knowledge content and use the same materials, but the latter can be in different forms according to the delivery method. For example, pictures of tooth anatomy will be used in all three delivery methods, a toothbrush will be shown as a picture in the lecture and the real product will be presented in the exhibition and demonstration, and toothbrushing practice will be presented as pictures/videos in the lecture and exhibition and a live demo during the demonstration.
OHEM-L: The lecture is a live talk by an educator aided by Power Point slides based on OHEM and delivered to a group of 20 participants/session for 30- to 40 minutes with no Q&A sessions.
OHEM-E: The exhibition is a display of educational posters and real exhibits based on OHEM. The participants will be given instructions to carry out self-learning by observing and reading the information. The participants will view the exhibits as they arrive but with some crowd control. The exhibition session would take 30-40 minutes to complete with no explanation by an educator and no Q&A at the end of the session.
OHEM-D: The demonstration is a live presentation by an educator with the aid of posters, actual products, and tooth models, and a live demo of toothbrushing, dental flossing, and mouth rinsing techniques based on OHEM. The demonstration will be delivered to a group of n=10 participants/ session for 30 - 40 minutes without a Q&A session.
All participants in the intervention groups will be instructed to teach their children what they have learned with the help of the booklet. Participants will also be taught how to teach their children.
Control: This group will not receive any intervention. However, they will be provided with an oral health education booklet without instructions to teach their children at home and an oral hygiene kit.
There will be no specific Q & A session for all groups. However, to keep the trial pragmatic and encourage a knowledge-seeking attitude among the mothers, the educator will respond to the queries if participants have any and including facilitating with hands-on practice.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
The inclusion criteria of the study are based on mothers and children.
Inclusion criteria
for Mothers:
Exclusion criteria
for mothers:
Inclusion criteria
for Children:
Exclusion criteria
for Children:
OHEM via lecture will be delivered to the mothers by an oral health professional who will be instructed to teach their children.
OHEM via exhibition will be delivered to the mothers who will be instructed to teach their children.
OHEM via demonstration will be delivered to the mothers by an oral health professional who will be instructed to teach their children.
Time frame: six months
i. Are you satisfied with the program's organisation? ii. Are you satisfied with the researcher's attitude during the trial? iii. Are you satisfied with the recruitment process? iv. Are you satisfied with the intervention process? v. Are you satisfied with the content taught during the intervention? vi. Are you satisfied with the researcher's delivery of the content? vii. Are you satisfied with arranging the OHEM sessions at the venue? viii. Is the environment at the venue conducive to learning? ix. Are you satisfied with the baseline and final stage of the oral screening process? x. Do you trust the researcher that her research will be fruitful for you and your family? The satisfaction will be assessed using a 10-item questionnaire mentioned in the primary objective. Participants will respond to each question using a 5-point Likert scale rating; each item will be reported as the percentage of participants who are at least somewhat satisfied (score 3,4,5)
Time frame: six months
i) How well participants cooperated
Additional comments by the researcher:______________________
The recruitment will be assessed on a Likert scale rating (very dissatisfied, dissatisfied, somewhat satisfied, satisfied, very satisfied); each item will be reported as the percentage of participants who are at least somewhat satisfied (score 3,4,5), whereas the participation of the participants will be assessed in percentage.
Time frame: six months
The cost of the trial will be assessed by comparing the cost of the expenditure at the end of the trial. i) Travelling cost, ii) Preparation of materials for the OHEM lecture, exhibition, and demonstration session cost, iii) Conducting the OHEM lecture, exhibition, and demonstration sessions cost, iv) Cost of the incentives for the participants, v) Cost for the volunteers of the trial.
Time frame: six months
Change in dental plaque scores among mothers and children between intervention and control groups, assessed pre- and post-intervention, using mean and Standard Deviation; lower scores will indicate good oral hygiene.
Time frame: six months
Change in gingival scores among mothers and children between intervention and control groups, assessed pre- and post-intervention, using mean and Standard Deviation; lower scores will indicate good oral hygiene.
Time frame: six months
Change in oral health KAP scores among mothers and children between intervention and control groups, assessed pre and post-intervention, using mean and Standard Deviation; the higher scores indicate better KAP.
Time frame: six months
Change in skills (tooth brushing and dental flossing) among mothers and children between intervention and control groups, assessed pre- and post-intervention, using add scores; higher scores indicate good behaviours.
Time frame: six months
Change in oral health impact profile-14 among mothers and children between intervention and control groups, assessed pre- and post-intervention, using add scores and mean and Standard Deviation; higher scores indicating poor oral health.
Contact information is provided by the study sponsor or research team.
Basaruddin Ahmad, PhD
CONTACT
Shahkamal Hashmi, PhD
CONTACT
Ziauddin University
Other
A Feasibility Study of the Investigation on the Efficacy of Oral Health Education for Mothers (OHEM) Module for Improving Oral Hygiene in Children.
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