- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05545254
Health-promoting Lifestyle in a Genetic Counseling Clinic
Health-promoting Lifestyle of Breast Cancer Patients and Family Members in a Chinese Genetic Counseling Clinic: A Cross-sectional Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Purpose: This study aimed to describe the health-promoting lifestyle of breast cancer patients and family members in a Chinese genetic counseling clinic, and to explore its various levels with different socio-economic variables.
Method: This was a cross-sectional study. The participants in this study originated from a genetic counseling clinic of a cancer center in Shanghai, China. 259 patients conformed to the inclusion and exclusion criteria were screened and contact from November 2019 to March 2022. Participants agreed to participate were sent a questionnaire web-link to be invited to finish this survey. Two questionnaires were included in the link, one referring to the socio-economic information, the other referring to the health-promoting lifestyle. Chinese Health-promoting lifestyle profile-Ⅱ(HPLP-Ⅱ) was used to evaluate the health-promoting lifestyle.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Shanghai, China
- Fudan University Shanghai Cancer Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- over 18 years old;
- with a diagnosis of breast cancer or having a family history of breast cancer
- the first time to take genetic testing in our clinic
- ECOG<2.
Exclusion Criteria:
- diagnosed with psychiatric or intellectual impairment
- having a history of genetic testing previously
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Breast cancer patients and their family members who have undertaken genetic testing
In this study, 259 participants were recruited from November 2019 to March 2022.
All participants originated from a genetic counseling clinic of a cancer center in Shanghai, China.
259 participants were contact, and among them, 158 participants finally agreed to participate and completed the survey.
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Two questionnaires were included in the link, one referring to the demographic information, and another one involving the health-promoting lifestyle.
In the demographic information, the genetic test results were not requested to be written, but the participants need to answer whether they understand the results.
The HPLP-Ⅱ is an scale instrument used to evaluate a person's health-promoting lifestyle behaviors, which contains 52 items and has been translated into Chinese in 1997.
It contains 6 subscales: self-actualization, health responsibility, physical activity, nutrition, interpersonal relationships and stress management.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Chinese Health-promoting lifestyle profile-Ⅱ
Time Frame: The primary outcome was measured during one month after the genetic test.
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HPLP-Ⅱ is an scale instrument used to evaluate a person's health-promoting lifestyle behaviors, which contains 52 items and has been translated into Chinese in 1997.It contains 6 subscales: self-actualization, health responsibility, physical activity, nutrition, interpersonal relationships and stress management.
A Likert 4-scale is used to measure each item, and never to regularly signifies 1-4.
The total score ranges from 52 to 208.
Higher scores mean better health-promoting behaviors.
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The primary outcome was measured during one month after the genetic test.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Zhenqi Lu, Master, Fudan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FNF201830
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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