Educational Videos for Thyroid Surgery Patient

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorWest China Hospital

About this trial

The researchers aim to evaluate the performance of two groups of participants after receiving traditional education-one group supplemented with video-based education and the other without. This study will explore the feasibility of using guideline-based public education videos on postoperative TSH suppression therapy for differentiated thyroid cancer in the context of public education regarding thyroid surgery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients scheduled for thyroid surgery, aged between 18 and 60 years old

Disqualifiers

Unable to read and write, pregnant, or with a history of thyroid surgery;

suffering from other malignant tumors or mental disorders;

unable to complete the questionnaire independently or requiring assistance from others.

Trial design

Design model

Single group

Treatments tested in this trial

  • Thyroid Surgery Educational Video

    Other intervention

    Accepting educational video on postoperative TSH suppression therapy for differentiated thyroid cancer created by researchers based on guidelines

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 1 intervention
Group B: Non-intervention groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

TSH Compliance Rate

The criteria for determining the TSH target achievement rate are based on a combination of three factors: the patient's postoperative recurrence risk stratification, the follow-up time point, and the current TSH test result. Within one year postoperatively, the TSH suppression targets are \< 0.1 mU/L for the high-risk group, 0.1-0.5 mU/L for the moderate-risk group, and 0.1-0.5 mU/L (low Tg) or 0.5-2 mU/L (undetectable Tg, lobectomy) for the low-risk group. In statistical analysis, the TSH target range attainment rate = (number of patients with TSH levels within the target range at each follow-up time point / total number of patients followed up at that time point) × 100%

Time frame
Postoperative Month 1, Postoperative Month 3, Postoperative Month 6, and Postoperative Month 12
2

Patient satisfaction

Patient satisfaction following different educational approaches was assessed using a 5-point Likert scale (1-5 scale; the higher the score, the higher the satisfaction).

Time frame
Immediately after the educational presentation (post-intervention)

Secondary outcomes

1

Level of knowledge dissemination

Knowledge assessment consists of 6 multiple-choice questions, 2 true/false questions, and 2 fill-in-the-blank questions to evaluate patients' understanding and awareness of educational topic.

Time frame
Postoperative Month 1, Postoperative Month 3, Postoperative Month 6, and Postoperative Month 12
2

Patient anxiety level

Anxiety scale, thereby assessing the patient's level of anxiety. A 5-point Likert scale was used, with each item scored on a scale of 1 to 5, ranging from "not at all" to "very severe."

Time frame
Baseline (before the educational outreach) and immediately after the educational outreach; two assessments total
3

Patient's Level of Regret After Surgery

Regret Scale, thereby recording the patient's degree of postoperative regret. 1. This was the right decision. 2\. I regret making this choice. 3. If I had the chance to do it over, I would make the same choice. 4. This choice caused me a lot of pain. 5. This was a wise decision. A 5-point Likert scale was used, with each item scored on a scale of 1 to 5; the lower the score, the less regret the respondent felt.

Time frame
Baseline (before the educational outreach) and immediately after the educational outreach
4

Incidence of adverse events in patients

Whether the patient has forgotten to take medication or mistakenly recorded the follow-up appointment time, etc.

Time frame
Postoperative Month 1, Postoperative Month 3, and Postoperative Month 6

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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