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New nursing approach may ease emotional toll of facial paralysis after brain surgery

NCT ID NCT07305285

Symptom relief Sponsor: West China Hospital Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a 12-week nursing program based on the Roy Adaptation Model in 160 adults who developed facial paralysis after surgery for a large acoustic neuroma. The program included education, counseling, and facial exercises, and aimed to reduce anxiety and depression while improving quality of life. Researchers also measured stress and inflammation markers in the blood. The goal was to see if this extra support helps people cope better than standard care alone.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

160 people

The number who actually took part.

Started

Jan 2022

Finished

Dec 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Confirmed GAN by preoperative MRI (tumor diameter \>4 cm) and postoperative pathological examination; * Postoperative facial paralysis diagnosed by neurological examination, with House-Brackmann (HB) grade ≥Ⅱ; * Age 18-65 years; * Conscious, with normal cognitive function (Mini-Mental State Examination score ≥24), able to communicate and complete questionnaires independently; * No history of psychological disorders or antidepressant/anxiolytic use before surgery; * Signed informed consent. Exclusion Criteria: * Preoperative facial paralysis, facial nerve palsy, or other facial muscle diseases; * History of schizophrenia, bipolar disorder, or other mental illnesses; * Severe postoperative complications (e.g., intracranial infection, hemorrhage, cerebrospinal fluid leakage) requiring reoperation; * Pregnancy or lactation; * Severe liver, kidney, or cardiovascular diseases; * Loss to follow-up or refusal to participate in the study.

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Conditions

The condition(s) this trial relates to.

acoustic neuroma facial paralysis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Acoustic neuroma Facial paralysis

Contacts and locations

Locations

  • West China Hospital

    Chengdu, Sichuan, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.