Sleep Disorders Trial, Recruiting NCT06975384 Sponsor: Second Xiangya Hospital of Central South University Condition: Sleep Disorders
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Sleep Disorders Trial, Recruiting

NCT06975384
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Cohort 1 (Non-small cell lung cancer – advanced, treated with immunotherapy)

Who might be able to join this trial:

  • Adults aged 18 or older
  • People with a confirmed diagnosis of non-small cell lung cancer (NSCLC), a common type of lung cancer
  • People whose cancer is at an advanced or spread stage (stage IIIB–IV) and cannot be removed by surgery
  • People whose general health and ability to carry out daily activities falls within a certain range, as measured by a standard scale (ECOG score of 0 or 1 — meaning fully active or able to carry out light work)
  • People who have not yet received any treatment for their cancer
  • People whose cancer has at least one measurable tumour, as defined by standard imaging guidelines
  • People who are receiving a type of cancer treatment called a PD-1/PD-L1 inhibitor (an immunotherapy drug), either alone or combined with chemotherapy
  • People who have given written consent to take part in the study

Who may not be able to join:

  • People whose cancer has specific gene changes known as EGFR-sensitising mutations, ALK fusions, or ROS1 fusions
  • People who have had another cancer diagnosis within the past 3 years
  • People currently living with an acute or ongoing mental health condition
  • People currently taking sleep medication
  • People who have previously taken part in another clinical drug trial
  • People who have brain metastases (cancer spread to the brain) that are causing symptoms
  • People who are unable to complete questionnaire-based assessments

Cohort 2 (Small cell lung cancer – advanced, treated with immunotherapy)

Who might be able to join this trial:

  • Adults aged 18 or older
  • People with a confirmed diagnosis of small cell lung cancer (SCLC)
  • People whose cancer is at an advanced or spread stage (stage III–IV) and cannot be removed by surgery
  • People whose general health falls within a certain range (ECOG score of 0 or 1)
  • People who have not yet received any treatment for their cancer
  • People whose cancer has at least one measurable tumour, as defined by standard imaging guidelines
  • People who are receiving a PD-1/PD-L1 inhibitor (an immunotherapy drug), either alone or combined with chemotherapy
  • People who have given written consent to take part in the study

Who may not be able to join:

  • People who have had another cancer diagnosis within the past 3 years
  • People currently living with an acute or ongoing mental health condition
  • People currently taking sleep medication
  • People who have previously taken part in another clinical drug trial
  • People who have brain metastases that are causing symptoms
  • People who are unable to complete questionnaire-based assessments

Cohort 3 (Non-small cell lung cancer – earlier stage, receiving pre-surgery immunotherapy)

Who might be able to join this trial:

  • Adults aged 18 or older
  • People with a confirmed diagnosis of non-small cell lung cancer (NSCLC)
  • People whose cancer is at a stage that may be removable by surgery (stage IB–IIIB)
  • People whose cancer has at least one measurable tumour, as defined by standard imaging guidelines
  • People who have not yet received any treatment for their cancer
  • People who are receiving a PD-1/PD-L1 inhibitor (an immunotherapy drug), either alone or combined with chemotherapy, as treatment before planned surgery
  • People whose heart and lung function is considered strong enough to tolerate surgery
  • People who have given written consent to take part in the study

Who may not be able to join:

  • People whose cancer has specific gene changes known as EGFR-sensitising mutations, ALK fusions, or ROS1 fusions
  • People who have had another cancer diagnosis within the past 3 years
  • People currently living with an acute or ongoing mental health condition
  • People currently taking sleep medication
  • People who have previously taken part in another clinical drug trial
  • People who have brain metastases that are causing symptoms
  • People who are unable to complete questionnaire-based assessments

Cohort 4 (Non-small cell lung cancer – early stage, treated with surgery)

Who might be able to join this trial:

  • Adults aged 18 or older
  • People with a confirmed diagnosis of non-small cell lung cancer (NSCLC)
  • People whose cancer has been confirmed at an early stage (stage IA–IIIA)
  • People for whom a tumour tissue sample is available
  • People who have not yet received any treatment for their cancer
  • People who are receiving surgery with the intent to fully remove the cancer
  • People who have given written consent to take part in the study

Who may not be able to join:

  • People who have had another cancer diagnosis within the past 3 years
  • People currently living with an acute or ongoing mental health condition
  • People currently taking sleep medication
  • People who have previously taken part in another clinical drug trial
  • People who are unable to complete questionnaire-based assessments

Cohort 5 (Non-small cell lung cancer – advanced, treated with targeted therapy)

Who might be able to join this trial:

  • Adults aged 18 or older
  • People with a confirmed diagnosis of non-small cell lung cancer (NSCLC)
  • People whose cancer is at an advanced or spread stage (stage IIIB–IV) and cannot be removed by surgery
  • People whose general health falls within a certain range (ECOG score of 0 or 1)
  • People who have not yet received any treatment for their cancer
  • People whose cancer has at least one measurable tumour, as defined by standard imaging guidelines
  • People who are receiving a targeted therapy drug, either alone or combined with chemotherapy
  • People whose cancer has a specific gene change (called a "driver gene mutation") that targeted therapy is designed to treat
  • People who have given written consent to take part in the study

Who may not be able to join:

  • People who have had another cancer diagnosis within the past 3 years
  • People currently living with an acute or ongoing mental health condition
  • People currently taking sleep medication
  • People who have previously taken part in another clinical drug trial
  • People who have brain metastases that are causing symptoms
  • People who are unable to complete questionnaire-based assessments

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +86 13574858332

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Second Xiangya Hospital of Central South University
Registry
ClinicalTrials.gov
Start date
1 November 2024
Est. completion
31 December 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Cohort 1 & 5: Progression-free survival (PFS); Cohort 2: Overall survival (OS); Cohort 3: Event-free survival (EFS); Cohort 4: Disease-free survival (DFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov