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Effects of Mobile-based Mindfulness Intervention to Reduce Preoperative Anxiety for Patients Undergoing Elective Surgery

RECRUITINGN/ASponsored by Hospital Authority, Hong Kong
Actively Recruiting
PhaseN/A
SponsorHospital Authority, Hong Kong
Started2025-06-13
Est. completion2025-12-31
Eligibility
Age18 Years+
Healthy vol.Accepted

Summary

This study is a pilot randomized controlled trial (RCT) conducted at Tin Shui Wai Hospital to evaluate the effectiveness of a mobile-based mindfulness intervention in reducing preoperative anxiety among patients scheduled for elective surgery. Aim: To determine if a 4-week mindfulness program delivered via a mobile app can reduce preoperative anxiety, compared to standard care. Design: Parallel-arm RCT with 40 participants (20 in each group). Participants are randomly assigned to either the intervention group (mobile-based mindfulness intervention + usual care) or control group (usual care only). The intervention uses a free and anonymous mindfulness mobile app developed by The University of Hong Kong. Primary Outcome: Preoperative anxiety level on the day of surgery, will be assessed using the STAI-S questionnaire. Secondary Outcomes: Postoperative pain levels, use of analgesics, emergency department revisit rate, and user satisfaction with the app. Data Collection: Anxiety levels are measured at baseline and before surgery. Pain levels and analgesic use are recorded postoperatively. Emergency visits and usability feedback are collected post-discharge. Significance: The study addresses a gap in evidence for mobile mindfulness interventions in Chinese surgical patients. Findings may support the integration of low-cost, app-based mindfulness into preoperative care.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

* adult (age\>= 18 years old)
* scheduled to undergo non-emergency surgery under general anesthesia (GA)
* use of smart phone
* able to understand the Chinese language and express their feelings sufficiently
* STAI-T score \>=40

Exclusion Criteria:

* unable to provide informed consent
* history or current treatment for psychological complaints
* serious physical or psychological co-morbidities
* hearing or vision impairment
* patients withdrawal from continuing to participate in the study

Conditions5

AnxietyMobile-based Mindfulness Intervention to Reduce Preoperative AnxietyPostoperative PainPostoperative Use of AnalgesicsPre-operative Anxiety

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