DBSOS: Evaluation of Interest of a Systematic Screening for Oncological Supportive Care Needs

Sponsor
Centre Paul Strauss (Other)
Overall Status
Completed
CT.gov ID
NCT03951701
Collaborator
(none)
134
1
1
4
33.2

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Evaluation of the supportive care
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
134 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Evaluation of Interest of a Systematic Screening for Oncological Supportive Care
Actual Study Start Date :
Sep 17, 2018
Actual Primary Completion Date :
Dec 5, 2018
Actual Study Completion Date :
Jan 18, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: observation cohort

Questionnaire to assess the supportive care needs

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

Outcome Measures

Primary Outcome Measures

  1. Evaluation of using oncological supportive cares after evaluation of supportive care needs reviewed by a professional of health, by a phone call [4 to 6 weeks after baseline]

    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)).

Secondary Outcome Measures

  1. Evaluation of initial supportive care needs by the self-assessment questionnaire [baseline]

    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).

  2. Assess the correlation between supportive care needs and age [This analyse will be realized at the end of the study (9 weeks after baseline)]

    Correlate the percentage of supportive care needs to age by a Pearson Chi squared test

  3. Assess the correlation between supportive care needs and sexe [This analyse will be realized at the end of the study (9 weeks after baseline)]

    Correlate the percentage of supportive care needs to sexe by a Pearson Chi squared test.

  4. Assess the correlation between supportive care needs and type of cancer [This analyse will be realized at the end of the study (9 weeks after baseline)]

    Correlate the percentage of supportive care needs to the type of cancer by a Pearson Chi squared test

  5. Compare the percentage of using a supportive care professional judgement in regard to read and unread questionnaires by medical staff [This analyse will be realized at the end of the study (9 weeks after baseline)]

    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.

  6. Compare the percentage of using a supportive care professional judgement in regard to the function of the medical staff member [This analyse will be realized at the end of the study (9 weeks after baseline)]

    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

  7. Assess the percentage of requirement to the physician during the study [4 to 6 weeks after baseline (by a phone call, at the same time than the hetero-questionnaire)]

    Assess the percentage of requirement to the physician during the study by asking each patient (by phone call)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Paul Strauss Strasbourg France 67065

Sponsors and Collaborators

  • Centre Paul Strauss

Investigators

  • Principal Investigator: Véronique FRASIE, Md, Centre Paul Strauss

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Paul Strauss
ClinicalTrials.gov Identifier:
NCT03951701
Other Study ID Numbers:
  • 2018-02
  • 2018-A01425-50
First Posted:
May 15, 2019
Last Update Posted:
May 23, 2019
Last Verified:
May 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 23, 2019