Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Quality of Life After Dental Extraction (CONNECT)
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
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.
調査の概要
状態
条件
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：Sundar Ramalingam
- 電話番号：00966532092386
- メール：smunusamy@ksu.edu.sa
研究場所
-
-
Riyadh Region
-
Riyadh、Riyadh Region、サウジアラビア、11545
- College of Dentistry and Dental University Hospital, King Saud University Medical City
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：支持療法
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ：Standard Postoperative Care
Participants allocated to this arm will receive the department's standard postoperative care following dental extraction, consisting of verbal postoperative instructions from the treating clinician and a standardized written instruction sheet.
No additional telephonic or digital follow-up communication will be provided beyond the routine postoperative review.
This arm serves as the reference group for comparison with the intervention arms.
|
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.
|
|
実験的：Telephonic Follow-up
Participants allocated to this arm will receive standard postoperative verbal and written instructions in addition to structured telephone follow-up communication during the first postoperative week.
Telephone calls will reinforce postoperative instructions, including adherence to medications, oral hygiene, dietary recommendations, saline mouth rinses, smoking cessation, and management of common postoperative concerns.
The calls will also provide an opportunity for participants to ask questions regarding their recovery.
|
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.
|
|
実験的：Digital Follow-up
Participants allocated to this arm will receive standard postoperative verbal and written instructions together with structured digital follow-up communication during the first postoperative week.
Digital communication will be delivered via a secure mobile messaging platform and will include reminder messages, educational infographics, and short instructional videos to reinforce routine postoperative instructions.
Participants may also communicate questions related to their postoperative recovery through the same platform.
|
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.
|
|
実験的：Hybrid Telephonic and Digital Follow-up
Participants allocated to this arm will receive standard postoperative verbal and written instructions, along with structured telephone follow-up and digital communication during the first postoperative week.
Telephone calls and digital educational materials will reinforce postoperative instructions and provide participants with opportunities to clarify concerns during recovery.
This arm represents the highest level of postoperative communication support.
It will be compared with the other study arms to evaluate its effectiveness in improving compliance, clinical recovery, and oral health-related quality of life.
|
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 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.
|
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Patient compliance with postoperative instructions
時間枠：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.
|
Postoperative Day 7
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Postoperative pain intensity
時間枠：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.
|
6 hours, Postoperative Day 1, Day 3, and Day 7
|
|
Incidence of alveolar osteitis (dry socket)
時間枠：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.
|
Postoperative Day 3 and Day 7
|
|
Oral health-related quality of life
時間枠：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.
|
Baseline (preoperative) and Postoperative Day 7
|
|
Patient satisfaction with postoperative communication
時間枠：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.
|
Postoperative Day 7
|
協力者と研究者
スポンサー
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- E-22-6719
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。