ClinicalTrials.gg
Not yet recruitingNCT07823543Updated Sep 16, 2026

Educational Videos for Thyroid Surgery Patient

An interventional study of Thyroid Surgery Educational Video in Thyroid Cancer, Thyroid Nodule and TSH, sponsored by West China Hospital. Not yet recruiting. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-16.

Primary conditionThyroid NoduleRegistry: Thyroid NeoplasmsReclassifiedWhy we changed it
Registry
Thyroid Neoplasms — the first condition term the registry derived for this study.
ClinicalTrials.gg
Thyroid Nodule
Why
  1. The study's listed conditions name Thyroid Nodule, a narrower term within Thyroid Neoplasms.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by West China Hospital · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
400
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Thyroid Cancer
  • Thyroid Nodule
  • TSH
  • Education of Patients

Browse trials for

03

In context

Thyroid Nodule Reclassified

207 studies on the registry are indexed under Thyroid Nodule; 64 are open to participants now.

This study's planned enrollment of 400 is above the median of 75 across 121 interventional studies indexed under Thyroid Nodule.

Browse Thyroid Nodule studies →

Lead sponsor

West China Hospital is the lead sponsor of 501 studies on the registry; 246 are open to participants now.

Compared within Thyroid Nodule, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Thyroid Neoplasms. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Single group
Masking
Single (Outcomes assessor)
Enrollment
400 participants (estimated)

Study arms

  • Experimental
    Intervention group

    Accepting educational video on postoperative TSH suppression therapy for differentiated thyroid cancer produced by researchers in accordance with guidelines

    Other: Thyroid Surgery Educational Video

  • No intervention
    Non-intervention group

    Without any additional intervention

Interventions

  • OtherThyroid Surgery Educational Video

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

06

What researchers measure

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

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Oct 2026; primary completion for Dec 2027, 14 months later.

Of 67 non-industry interventional studies with no phase under Thyroid Nodule, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 46. This study's planned 14 months is below that.

Counting every sponsor, half of 71 studies reached it within 30 months; a quarter within 14 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 14, 2025
First posted
Sep 16, 2026
StartEst.
Oct 1, 2026
Primary completionEst.
Dec 1, 2027
CompletionEst.
Dec 1, 2027
Last update
Sep 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07823543
Responsible party
Jianyong Lei (Professor, West China Hospital) — Principal investigator
First posted
Sep 16, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Dec 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Sep 16, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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