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NCT07749443Completed

Construction and Empirical Study of Indirect Intervention Model for Protective Medical Lung Cancer Patients Based on Family System Theory

Source: ClinicalTrials.gov · Last updated 6 Aug 2026

Brief summary (registry, in English)

To clarify the irrational cognition of family caregivers of lung cancer patients at various perioperative stages under the background of protective medical treatment, construct an indirect intervention model for lung cancer patients, and evaluate its clinical efficacy. To develop popularizable cognitive intervention tools and formulate practical cognitive intervention strategies, so as to relieve perioperative stress responses among lung cancer patients and their family caregivers. To provide reliable evidence and research directions for carrying out comprehensive and systematic interventions on perioperative stress responses in lung cancer patients and their family caregivers in clinical practice in the future.

Status (registry)
Completed
Study type
Interventional
Enrollment
160 (actual)
First submitted
31 Jul 2026
Start date
1 May 2025
Primary completion date
31 Mar 2026
Lead sponsor
Anhui Medical University
Diseases
Lung cancer
NCT number
NCT07749443

What you commit to

  • Study type: Interventional
  • Participants enrolled: 160
  • From 1 May 2025 to the primary completion date, 31 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • (1)Patients:
    • Patients who do not meet the surgical indications as evaluated by clinicians;
    • Patients with immune system diseases;
    • Patients with a history of mental illness or severe cognitive impairment.
    • (2)Family Caregivers:
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    • Caregivers with severe organic lesions themselves;
    • Caregivers who have experienced other major life events recently;
    • Caregivers with a history of mental illness or severe cognitive impairment.

Who the study is looking for

  • (1)Patients
    • Eligible for radical lung cancer surgery confirmed by clinicians in accordance with lung cancer clinical guidelines;
    • Aged over 18 years old;
    • No history of drug or alcohol dependence, and no use of contraceptives or hormones within the past three months;
    • Fully informed of the study, signed informed consent and volunteered to participate.
    • (2)Family Caregivers
    • <!-- -->
    • Spouses, adult children or other relatives who provide long-term unpaid daily care and companionship for patients;
    • Aged over 18 years old;
    • No history of drug or alcohol dependence, and no use of contraceptives or hormones within the past three months;
    • Fully informed of the study, signed informed consent and volunteered to participate.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Anhui Provincial Hospital
Coordinator of this site? Confirm its status
HefeiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.