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Family support may be key to easing lung cancer surgery stress

NCT ID NCT07749443

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
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

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 06, 2026 · Last updated Aug 07, 2026 · Updated 1 time

Summary

This study tests whether teaching family caregivers about lung cancer care—through a handbook and personalized guidance—can reduce stress and improve quality of life for patients undergoing lung cancer surgery. The trial involves 160 patients and their caregivers, with some receiving the extra caregiver education and others standard care. Researchers will measure decision-making confidence, functional status, and anxiety and depression levels to see if this family-based approach helps.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Caregiver cognitive intervention using a printed handbook and graded information disclosure strategies
What this could lead to
If effective, this approach could provide a simple, low-cost way to reduce stress and improve recovery for lung cancer surgery patients by involving their families.
What could go wrong
The trial is relatively small and early-stage, so results may not apply broadly. The intervention depends on caregiver participation, which may vary, and benefits might be modest.

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

May 2025

Finished

Mar 2026

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 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * (1)Patients 1. Eligible for radical lung cancer surgery confirmed by clinicians in accordance with lung cancer clinical guidelines; 2. Aged over 18 years old; 3. No history of drug or alcohol dependence, and no use of contraceptives or hormones within the past three months; 4. Fully informed of the study, signed informed consent and volunteered to participate. (2)Family Caregivers <!-- --> 1. Spouses, adult children or other relatives who provide long-term unpaid daily care and companionship for patients; 2. Aged over 18 years old; 3. No history of drug or alcohol dependence, and no use of contraceptives or hormones within the past three months; 4. Fully informed of the study, signed informed consent and volunteered to participate. Exclusion Criteria: * (1)Patients: 1. Patients who do not meet the surgical indications as evaluated by clinicians; 2. Patients with immune system diseases; 3. Patients with a history of mental illness or severe cognitive impairment. (2)Family Caregivers: <!-- --> 1. Caregivers with severe organic lesions themselves; 2. Caregivers who have experienced other major life events recently; 3. Caregivers with a history of mental illness or severe cognitive impairment.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Anhui Provincial Hospital

    Hefei, Anhui, China

More trials for these conditions

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