Association of Psychological Distress in Patients With Lung Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Chest Hospital

About this trial

Psychological distress is a multi-factorial experience of a psychological, social, spiritual, and/or physical nature that may interfere with one's ability to cope effectively with cancer, physical symptoms and treatment. Psychological distress is common and affects the efficacy and prognosis of patients with lung cancer. The systematic anti-tumor therapy may effectively relieve psychological distress including anxiety, depression, and fatigue in patients with advanced lung cancer, the relief of the psychological distress can in turn improve the therapeutic effect.

In summary, this study is to explore the associations of (dynamic) psychological stress with the efficacy and survival of anti-tumor therapy including immunotherapy and targeted therapy for advanced lung cancer patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Histologically proven diagnosis of lung cancer

18 years of age or older

Ability to understand and the willingness to sign a written informed consent document

Disqualifiers

Not willing to participate in this clinical trial

Trial population

Participants with lung cancer are with the standard treatment and/or are enrolled in the clinical trials.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • immunotherapy

    Drug
  • Targeted Therapy Agent

    Drug

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Objective response rate (ORR)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years
2

Disease control rate (DCR)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years
3

Progression-free survival (PFS)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years

Secondary outcomes

1

Overall survival (OS)

Collect detailed clinical information on patients with SCLC via the electronic medical records

Time frame
20 years

Other outcomes

Sponsors and contacts

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