Effect of Mobile Health on Plaque Control Efficacy in Molars With Furcation Involvement

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorPostgraduate Institute of Dental Sciences Rohtak

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Behavioural text messages twice weekly

    Behavioral

    Regular messages twice a week will be sent to the individuals reminding the individuals for standardized oral hygiene instructions and interradicular brushing in furcation involvement. Individuals will be asked to respond to the messages.

  • Standardized oral hygiene instructions

    Other intervention

    All participants will recieve standardized oral hygiene instructions including toothbrushing techniques and interdental brushes.

Treatment groups

76 Participants
are divided into 2 treatment groups
Group A: Messages + Oral hygiene InstructionsExperimental treatment 2 interventions
Group B: Oral hygiene InstructionsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Plaque Index

Plaque index by Silness and Loe (1964) will be used for assessment of plaque.Score range of this index is from 0 to 3.Score 0 means good oral hygiene and score 3 means poor oral hygiene.

Time frame
6 months
2

Bleeding on probing

It will be measured by walking the periodontal probe at 6 sites of each tooth (mesio-buccal, mid-buccal, disto-buccal, mesio- lingual, mid-lingual and disto-lingual). It will be recorded as 1 (present) if it occurred within 15 sec of probing and 0 (absent) if no bleeding occurred. It will be calculated in %.

Time frame
6 months

Secondary outcomes

1

PROBING POCKET DEPTH (PPD)

Probing pocket depth will be measured as the distance from gingival margin to the base of pocket. The probing depth measurements will be assessed using the Periodontal probe. The probe will be inserted in the bottom of pocket and maintained parallel to vertical axis of the tooth. Measurements will be noted at 6 sites of a tooth (mesio-buccal, mid-buccal, disto-buccal, mesio-lingual, mid-lingual and disto-lingual). Measurements will be rounded to the nearest whole millimeter.

Time frame
6 months
2

HORIZONTAL PROBING DEPTH (HPD)

Horizontal probing depth will be assessed by probing the furcation in a horizontal direction using a rigid curved probe (e.g. Nabers probe) and measuring the distance from the probe tip to a virtual tangent to the root convexities adjacent to the furcation. Measuring this distance allows assessment of different degrees of FI or the amount of horizontal attachment loss in millimeters (horizontal probing/ clinical attachment level: PAL-H/HCAL).

Time frame
6 months
3

VERTICAL PROBING DEPTH (HPD)

UNC-15 periodontal probe will be used to record the vertical depth. The probe will be inserted into the periodontal pocket up to the alveolar bone, and the distance from the roof of furcation to the vertical depth of probing (VD) will be measured. All measurements will be recorded nearest to the millimeter.

Time frame
6 months
4

CLINICAL ATTACHMENT LEVEL(CAL)

Clinical attachment level will be measured as the distance between the cemento-enamel junction and the base of pocket. Measurements will be made at 6 sites of each tooth (mesio-buccal, mid-buccal, disto-buccal, mesio- lingual, mid-lingual and disto-lingual) using Periodontal probe. Distance of base of the pocket from gingival margin, distance of free gingival margin from CEJ will be measured. Afterwards CAL will be calculated based on following criteria. When gingival margin is located on the anatomic crown, the level of attachment is determined by subtracting from the depth of pocket, the distance from the gingival margin to the CEJ. If both are same, the loss of attachment is recorded as zero. When gingival margin coincides with CEJ, the loss of attachment equals to probing pocket depth. When gingival margin is located apical to CEJ, the loss of attachment is greater than probing depth and therefore the distance between CEJ and gingival margin is adde

Time frame
6 months

Other outcomes

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