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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03951701
Other study ID # 2018-02
Secondary ID 2018-A01425-50
Status Completed
Phase N/A
First received
Last updated
Start date September 17, 2018
Est. completion date January 18, 2019

Study information

Verified date May 2019
Source Centre Paul Strauss
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Monocentric, descriptive, cross-sectional, interventional, prospective and non-randomized study.


Description:

The study will unfold in the followed day hospital's departments of the Paul Strauss Cancer Center (Strasbourg, France) : supportive care department, chemiotherapy department and radiotherapy department. The study is based on two questionnaires that include six sections : nutrition, social, psychologic, physiotherapy, pain and supportive care needs evaluation.

The first questionnaire gives information about the patient and allow to screen supportive care needs. It should be read by medical or paramedical staff who report the function of the reader and options that are proposed to the patient after reading the questionnaire.

The second questionnaire will be done after 4 to 6 weeks by a phone call from the clinical research nurse. The objective of this questionnaire is to determine what kind of care have been provided.


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date January 18, 2019
Est. primary completion date December 5, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient treated for a cancer

- Age = 18 years old

- Receiving treatment (chemotherapy and/or radiotherapy) in day hospital and/or supportive care department

- Able to speak, read and understand French

- Able to communicate by phone

- Written informed consent obtained from the patient

- Registration in a national health care system

Exclusion Criteria:

- Minor or protected adult

- Pregnant or breastfeeding woman

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Evaluation of the supportive care
Evaluation of interest of a systematic screening for oncological supportive care needs

Locations

Country Name City State
France Centre Paul Strauss Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
Centre Paul Strauss

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of using oncological supportive cares after evaluation of supportive care needs reviewed by a professional of health, by a phone call Assess the percentage of using oncological supportive cares after evaluation of supportive care needs reviewed by a professional. The use of supportive cares is evaluated with an hetero-questionnaire created for this study. The hetero-questionnaire consists in a phone call to evaluate the evolution of each item of the self-assessment questionnaire (which includes 6 evaluations : a nutritional evaluation (10 items), a social evaluation (8 items), a psychologic evaluation (6 items), a physiological evaluation (7 items), a pain evaluation (4 items) and a supportive care needs evaluation (6 items)). 4 to 6 weeks after baseline
Secondary Evaluation of initial supportive care needs by the self-assessment questionnaire Assess the percentage of initial supportive care needs evaluated by the self-assessment questionnaire created for this study. It includes evaluations : a nutritional evaluation (10 items), a social evaluation (8 items), a psychologic evaluation (6 items), a physiological evaluation (7 items), a pain evaluation (4 items) and a supportive care needs evaluation (6 items). baseline
Secondary Assess the correlation between supportive care needs and age Correlate the percentage of supportive care needs to age by a Pearson Chi squared test This analyse will be realized at the end of the study (9 weeks after baseline)
Secondary Assess the correlation between supportive care needs and sexe Correlate the percentage of supportive care needs to sexe by a Pearson Chi squared test. This analyse will be realized at the end of the study (9 weeks after baseline)
Secondary Assess the correlation between supportive care needs and type of cancer Correlate the percentage of supportive care needs to the type of cancer by a Pearson Chi squared test This analyse will be realized at the end of the study (9 weeks after baseline)
Secondary Compare the percentage of using a supportive care professional judgement in regard to read and unread questionnaires by medical staff Assess the percentage of using a supportive care when the medical staff read the completed questionnaire. Assess the percentage of using a supportive care when the medical staff didn't read the completed questionnaire. Then compare these values by using a T- test of Student. This analyse will be realized at the end of the study (9 weeks after baseline)
Secondary Compare the percentage of using a supportive care professional judgement in regard to the function of the medical staff member Assess the percentage of using a supportive care when the medical staff who read the completed questionnaire is a doctor, a nurse, or an auxiliary nurse . Then compare these values by using a T- test of Student This analyse will be realized at the end of the study (9 weeks after baseline)
Secondary Assess the percentage of requirement to the physician during the study Assess the percentage of requirement to the physician during the study by asking each patient (by phone call) 4 to 6 weeks after baseline (by a phone call, at the same time than the hetero-questionnaire)
See also
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