Establishment of a Decision Aid Tool for Asymptomatic Small Leiomyoma and Analysis of Influencing Factors for Clinical Decision-making Using HIFU

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-55
SponsorShenzhen Maternity & Child Healthcare Hospital

About this trial

With the younger patients diagnosed with asymptomatic leiomyoma, delay in the reproductive age of women, the advancement of medical technology, and the rapid development of treatment methods, there are many choices between gynecologists, gynecologists and patients because of experience and knowledge. It is not easy to make the most favorable choice for patients. This study is mainly led by a committee composed of designers, doctors, nurses and patients, and based on clinical guidelines and evidence-based medicine. Co-operating with patients with asymptomatic small leiomyoma, we want to find the influencing factors of clinical decision-making, and to establish a patient decision aid tool. We use prospective trial to verify that the use of this tool can improve patients' decision-making efficacy and further improve patient-reported outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of leiomyoma: patients with leiomyoma diagnosed by imaging examinations (ultrasound and MRI) have no clinical symptoms;

Female with age in 18-55 years old;

The maximum diameter of a single leiomyoma is less than 5m, and the number does not exceed 10 by MRI;

No contraindications for sedation and analgesia;

Disqualifiers

History of myomectomy, including transabdominal, laparoscopic, hysteroscopy, etc.;

History of connective tissue diseases or radiotherapy, especially abdominal radiotherapy;

With pregnancy, acute inflammation of the reproductive tract, or other gynecological benign and malignant diseases such as endometriosis and ovarian tumors;

The maximum diameter of leiomyoma is greater than or equal to 5cm;

Trial population

18-55 years old woman diagnosed with uterine fibroids and without clinical symptoms

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Patients Decision Aids

    Other intervention

    Patient Decision Aids (PDAs) are an important way to facilitate making decision by patients, helping patients make specific and prudent choices by providing information about treatment options and corresponding outcomes, including benefits and risks, related to their health status. The purpose of PDAs is to encourage patients to participate in decision-making. It makes it easier for patients and doctors to discuss treatment options. It effectively promotes communication between patients and doctors. It can help patients combine their own needs and professional advice to make better, more individualized diagnosis and treatment options.

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: communication without PADs0 interventions
Group B: communication with PADs1 intervention

Trial outcomes

Primary outcomes

1

Patient satisfaction after using PDAs

The patients in PDAs will undertake the treatment by PDAs. And we will collect the satisfaction after 12 months.

Time frame
6-12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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