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NCT Number: NCT05339568

Patient's Whole Process Follow-up Management(HOPE-1)

Our project is going to explore whether management and follow-up of locally advanced/metastatic patients using the patient process management platform can prolong patient survival and improve patient quality of life.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The First Affiliated Hospital of Shandong First Medical University

Jinan, Shandong, China

Location status: Recruiting

Location contact

Jiandong ZHANG

CONTACT

[email protected]

+8653189268118

About this study

Now, the treatment of NSCLC is diversiform, such as radiation and chemotherapy, targeted therapy, immune therapy, the treatment goal is to reduce symptoms, improve quality of life, prolong life. But as a result of the disease itself has the high risk of metastasis and recurrence. The treatment is often accompanied by a series of complications, if the patients don't get medical assistance in time, it will lead high risk to physical and mental health of patients. In China, the intermittent period of domestic treatment is mainly family recuperation, but due to the lack of medical knowledge or self-management and self-restraint ability of patients, they may forget to take medicine, stop medication without permission due to side effects and other behaviors that do not follow the doctor's advice, the poorly patients' compliance will lead to a significant reduction in the treatment effect. NSCLC are often accompanied by anxiety, fear, insomnia and other symptoms, causing a huge psychological burden on patients and their families, affecting the quality of life. Whole process follow-up in tumor therapy plays an important role , it is the crucial link between medical, nursing, and patients. Patients' whole process follow-up and management is an important part of cancer disease management.

It is helpful to relieve the patients and their families of the bad psychology, reduce the symptoms of patients, improve the patient's compliance behavior, relieve the psychological anxiety of patients, make it actively cooperate with the treatment, reduce complications, improve the quality of life of patients, so as to prolong the life cycle.

Our project is going to explore whether management and follow-up of locally advanced/metastatic patients using the patient process management platform can prolong patient survival and improve patient quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fully understand the research and voluntarily sign the informed consent form (ICF)
  • Male or female subjects who are over 18 years old (inclusive) at the time of signing the informed consent form.
  • The subject is diagnosed pathologically or cytologically with non-small cell lung cancer(NSCLC).
  • According to the 8th edition of the American Joint Committee on Cancer [AJCC], it is classified as stage IIB, stage III, stage IV NSCLC.
  • Not suitable for radical treatment or refuse surgery.
  • The life expectancy is not less than 3 months.
  • Be able to use a smartphone.

Exclusion criteria

  • Patients with mental illness.
  • Presence of any other malignant tumor.
  • Patients who are expected to undergo radical surgery.
  • Currently participating in clinical trials.
  • Subjects who judged by the investigator to be unsuitable to participate in the trial.

Treatment and study plan

Patients' whole process follow-up and management platform

Other

Patients' whole process follow-up and management platform is a software for the patients and investigators. This platform will use to collect patients' information when they are out of patients and will provide the patients' education materials.

Primary outcomes

  1. Overall survival time

    Time frame: UP to 96 months

    OS was calculated from the date of randomization to death from any cause.

Secondary outcomes

  1. Progression-free survival (PFS)

    Time frame: Up to 96 months

    PFS was calculated from date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 96 months.

  2. Adverse events rate

    Time frame: Up to 96 months

    Adverse events were assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0.

  3. Patients' follow-up compliance

    Time frame: Up to 96 months

    Patients' follow-up compliance were assessed by the N of hospital visits according to the doctors' advice every year.

  4. The quality of life

    Time frame: Up to 96 months

    The quality of life were assessed by SF-36,The SF-36 questionnaire consists of 8 section, including physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, mental health, also including reported health transition. The scoring steps: 1 encode the scale 2 credit the scale 3 score conversion(conversion formula=(actual score-the possible lowest score of this section)/the difference between the possible highest score and the possible lowest score of this section).The higher the score conversion, the better the health.

  5. Follow-up satisfaction

    Time frame: Up to 96 months

    Follow-up satisfaction were assessed by the questionnaire. The questionnaire is including 12 questions, where 28 is the worst imaginable satisfaction state and 130 is the best imaginable satisfaction state.

Study contacts

Contact information is provided by the study sponsor or research team.

Jiandong ZHANG

CONTACT

[email protected]

(+86531)89268118

Sponsors and collaborators

Lead sponsor

Qianfoshan Hospital

Other

Registry information

Official study title

A Multicenter, Randomized, Open, Parallel Grouping, Investigator-initiated Study Evaluating the Long-term Benefit of Patients With Locally Advanced/Metastatic Non-small Cell Lung Cancer Followed up Using a Patient-wide Management Platform

Acronym: HOPE-1

Important dates

Study start
2022
Primary completion
2030
Study completion
2030
First posted
Apr 21, 2022
Registry last updated
Sep 8, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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