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Recruiting NCT07707401

Effectiveness of WeChat-Supported Neck Rehabilitation Exercises on Early Recovery After Thyroidectomy

No phase Interventional Thyroid Diseases Thyroid Cancer Surgery Postoperative Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: WeChat-supported Neck Rehabilitation Exercise, Standardized Postoperative Care and Video Education.
Who it may be relevant to
Registry conditions: Thyroid Diseases, Thyroid Cancer, Surgery, Postoperative Pain. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effectiveness of WeChat-Supported Neck Rehabilitation Exercises on Early Recovery After Thyroidectomy: A Randomized Controlled Trial

Overview

This study aimed to evaluate the effectiveness, safety, and implementation outcomes of a WeChat mini program-supported tele-neck rehabilitation exercises for improving early postoperative neck recovery after thyroidectomy.

Interventions

  • Behavioral WeChat-supported Neck Rehabilitation Exercise
    WeChat mini program-supported neck exercise management includes daily exercise reminders, exercise check-ins, symptom reporting, automated abnormal symptom prompts, and standardized remote feedback from the research team.
  • Behavioral Standardized Postoperative Care and Video Education
    This intervention consists of standard clinical postoperative care and discharge education, encompassing wound management, follow-up appointments, and generic neck activity guidelines. Prior to discharge or upon clinical stability, participants undergo a one-time, face-to-face training session with research staff featuring practical exercise demonstrations and behavioral precautions, and are provided with identical instructional video materials for home reference.

Primary outcome measures

  • Neck Pain and Disability Scale (NPDS) Score [Time frame: Postoperative day 3, week 1, week 2, and month 1]
Secondary outcome measures (4)
  • Neck Movement Pain Score [Time frame: Postoperative day 3, week 1, week 2, and month 1]
  • Digital Health App Adherence and Feasibility Metrics [Time frame: Up to 1 month post-operation]
  • Incidence of Surgical Complications and Intervention-Related Adverse Events [Time frame: Up to 1 month post-operation]
  • Cervical Range of Motion (ROM) [Time frame: Postoperative week 1 and month 1]

Eligibility criteria

Inclusion criteria

  • Undergoing thyroid surgery
  • Postoperative condition stable, with the attending physician assessing the patient as fit for neck movement
  • Willing to participate in the study, complete scheduled follow-ups, and sign a written informed consent form

Exclusion criteria

  • History of prior thyroid or neck surgery
  • History of cervical spondylosis, cervical spine surgery, neck trauma, or other conditions affecting neck mobility
  • Postoperative complications rendering the patient unsuitable for neck movement training, such as confirmed recurrent laryngeal nerve injury, chyle leak, or complications requiring reoperation or prolonged drainage, or incision infection
  • Persistent postoperative dizziness or other conditions unsuitable for exercise
  • Unable to use WeChat and lacking assistance from family members

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

China · 1 center
  • Shanghai Sixth People's Hospital — Shanghai

Identifiers

NCT: NCT07707401 · 2026-KY-277(K)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗