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NCT Number: NCT07751822

Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Quality of Life After Dental Extraction

Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Oral Health-related Quality of Life Following Dental Extraction

(CONNECT Study - CONtinuous post-operative NETwork Communication to Enhance Compliance after Tooth Extraction)

Tooth extraction is one of the most commonly performed dental procedures. Although most patients recover uneventfully, complications such as pain, swelling, bleeding, infection, and dry socket may occur if postoperative instructions are not followed correctly. Dentists routinely provide verbal and written instructions after tooth extraction; however, patients may forget or misunderstand these instructions once they leave the clinic, resulting in reduced compliance and delayed recovery.

Previous research conducted at our institution demonstrated that postoperative telephone follow-up improved patient compliance with post-extraction instructions compared with routine verbal and written instructions alone. Building on these findings, the present study aims to evaluate whether different methods of postoperative communication-including telephone calls, digital messaging, and a combination of both-can further improve patient compliance and clinical recovery following dental extraction.

Participants undergoing routine dental extraction will receive the standard postoperative verbal and written instructions provided by the Department of Oral and Maxillofacial Surgery. Depending on the assigned study group, participants may also receive structured telephone follow-up, digital communication via a secure messaging platform, or both during the early postoperative period. The information provided through these communication methods will reinforce the same postoperative instructions routinely given in the clinic and will not alter the clinical treatment received.

Participants will be followed for one week after the extraction. Information will be collected regarding their adherence to postoperative instructions, pain levels, occurrence of complications such as dry socket, and oral health-related quality of life using validated questionnaires. These assessments will help determine whether additional postoperative communication improves patient recovery and overall treatment outcomes.

The study involves minimal risk because the communication methods are intended only to reinforce standard postoperative care and provide patients with an opportunity to clarify any concerns they may have during recovery. Participation in the study is entirely voluntary, and patients may withdraw at any time without affecting the quality of their dental treatment.

The findings of this study are expected to provide evidence on the most effective postoperative communication strategy following dental extraction. This may help improve patient education, enhance compliance with postoperative instructions, reduce preventable complications, and support the integration of digital communication technologies into routine dental practice.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

College of Dentistry and Dental University Hospital, King Saud University Medical City

Riyadh, Riyadh Region, 11545, Saudi Arabia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

- Participants must meet all of the following criteria:

Adults aged 18 years or older. Patients undergoing simple or surgical dental extraction under local anesthesia at the Department of Oral and Maxillofacial Surgery.

Able to understand and communicate in Arabic or English. Own a smartphone with access to a mobile messaging application (e.g., WhatsApp) and be able to receive telephone calls.

Willing and able to provide written informed consent. Willing to comply with the study protocol and attend the scheduled postoperative follow-up visits.

Exclusion criteria

- Participants meeting any of the following criteria will be excluded:

Patients younger than 18 years of age. Patients unable to provide informed consent. Patients with cognitive impairment, psychiatric illness, or neurological disorders that may interfere with understanding or complying with postoperative instructions.

Patients with hearing or speech impairment preventing effective telephone communication.

Patients without access to a smartphone or unable to use mobile messaging applications independently.

Patients requiring hospital admission following dental extraction. Patients undergoing extraction under general anesthesia. Patients who are unwilling or unable to complete the scheduled follow-up assessments.

Patients participating in another clinical trial that may influence postoperative recovery or study outcomes.

Treatment and study plan

Telephonic Postoperative Follow-up

Behavioral

Telephonic postoperative follow-up consists of structured telephone calls delivered by trained study personnel during the first postoperative week following dental extraction. Calls reinforce routine postoperative instructions, assess patient understanding, encourage adherence to medications and self-care recommendations, address common postoperative concerns such as pain or bleeding, and provide an opportunity for participants to ask questions regarding their recovery. A standardized communication script will be used to ensure consistency across participants.

Digital Postoperative Follow-up

Behavioral

Digital postoperative follow-up consists of structured communication delivered through a secure mobile messaging platform during the first postoperative week following dental extraction. Participants will receive standardized reminder messages, educational infographics, and short instructional videos that reinforce routine postoperative instructions on medication adherence, oral hygiene, diet, saline mouth rinses, smoking avoidance, and management of common postoperative symptoms. Digital communication will follow a predefined schedule and standardized content to ensure uniformity across participants.

Standard Postoperative Care

Behavioral

Standard postoperative care consists of routine verbal instructions provided immediately after dental extraction, along with a standardized written instruction sheet. The instructions include guidance on bleeding control, medication adherence, oral hygiene, dietary recommendations, saline mouth rinses, smoking avoidance, and measures to promote uncomplicated healing. No additional structured telephonic or digital follow-up communication is provided beyond the routine postoperative review.

Primary outcomes

  1. Patient compliance with postoperative instructions

    Time frame: Postoperative Day 7

    Patient compliance will be assessed using a structured postoperative compliance questionnaire evaluating adherence to standardized post-extraction instructions, including medication use, oral hygiene, saline mouth rinses, dietary recommendations, smoking avoidance, and clot protection. The total compliance score will be compared between the study groups.

Secondary outcomes

  1. Postoperative pain intensity

    Time frame: 6 hours, Postoperative Day 1, Day 3, and Day 7

    Postoperative pain will be measured using a 10-cm Visual Analogue Scale (VAS), where 0 represents no pain and 10 represents the worst imaginable pain.

  2. Incidence of alveolar osteitis (dry socket)

    Time frame: Postoperative Day 3 and Day 7

    The occurrence of alveolar osteitis will be assessed clinically using standardized diagnostic criteria, including increasing postoperative pain associated with partial or complete loss of the blood clot requiring clinical management.

  3. Oral health-related quality of life

    Time frame: Baseline (preoperative) and Postoperative Day 7

    Oral health-related quality of life will be assessed using the validated Oral Health Impact Profile-14 (OHIP-14) questionnaire. Changes in OHIP-14 scores from baseline will be compared among the study groups.

  4. Patient satisfaction with postoperative communication

    Time frame: Postoperative Day 7

    Participant satisfaction with the postoperative communication strategy will be evaluated using a structured questionnaire incorporating a five-point Likert scale assessing clarity of instructions, ease of communication, confidence during recovery, and overall satisfaction.

Study contacts

Contact information is provided by the study sponsor or research team.

Sundar Ramalingam

CONTACT

[email protected]

00966532092386

Sponsors and collaborators

Lead sponsor

King Saud University

Other

Registry information

Official study title

Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Oral Health-related Quality of Life Following Dental Extraction

Acronym: CONNECT

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 7, 2026
Registry last updated
Aug 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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