Effect of Mobile Health on Plaque Control Efficacy in Molars With Furcation Involvement (NCT07642895) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Mobile Health on Plaque Control Efficacy in Molars With Furcation Involvement
India76 participantsStarted 2026-06
Plain-language summary
Furcation involvement (FI) refers to a condition in which the progression of the periodontal disease process invades the bifurcation and trifurcation of multirooted teeth. Furcation involvement, present a clinical challenge due to its anatomic complexity and reduced access for adequate plaque control which may leads to further periodontal breakdown. Consequently, maintenance of adequate oral hygiene is critical in these sites.
It has been shown that poor oral hygiene, together with the persistence of periodontal risk factors, leads to further disease progression, treatment failure, and disease recurrence.
Mobile health can serve as a valuable adjunctive approach by aiding in behavioral reinforcement through real-time reminders. With widespread mobile phone usage in India, mHealth interventions are feasible. The role of mHealth in management of furcation involved sites has still not been explored. Therefore, this randomized controlled clinical trial aims to evaluate the effectiveness of mobile health reinforcements in improving plaque control efficacy at in furcation involved sites following non-surgical periodontal therapy, with the potential to enhance patient compliance and prevent further disease progression and disease recurrence.
Who can participate
Age range
18 Years – 55 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Systemically healthy individuals with clinically visible furcation entrance in mandibular molars in Stage III periodontitis
* Horizontal bone loss extent ≥ 3mm29 and vertical bone loss ( Subclass A/B)30
* Access to mobile phone
Exclusion Criteria:
* Presence of systemic diseases that could influence the outcome of periodontal therapy (Diabetes mellitus, Hypertension)
* Smoking/alcohol consumption
* Teeth with Grade II/III mobility
* History of periodontal treatment or antibiotic therapy in the last 6 months
* Non-vital and carious teeth to be restored
* Physically and mentally impaired patients
* Furcation involvement with cervical enamel projections, enamel pearls and bifurcation ridges
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Plaque Index
Timeframe: 6 months
2
Bleeding on probing
Timeframe: 6 months
Trial details
NCT IDNCT07642895
SponsorPostgraduate Institute of Dental Sciences Rohtak