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Impact of a Telephonic Monitoring During Inter-treatment Intervals on Emotional State, Quality of Life and Toxicities, on Neo Adjuvant or Adjuvant Chemotherapy-treated Patients (EMOTION)

Primary Purpose

Non-metastatic Patients With Breast Cancer, Non-metastatic Patients With Colon Cancer, Non-metastatic Patients With Rectal Cancer

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Clinical and psychosocial phone calls
Sponsored by
Centre Antoine Lacassagne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Non-metastatic Patients With Breast Cancer focused on measuring breast cancer, colon cancer, rectal cancer, adjuvant chemotherapy, phone calls, emotional states, quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient older than 18.
  • Patient surgically-treated or no for non inflammatory breast cancer or for colon cancer or rectal cancer.
  • Patient to be treated by neo-adjuvant or adjuvant chemotherapy by 5-fluorouracil, epirubicin and cyclophosphamide (FEC)-docetaxel, docetaxel-cyclophosphamide, 5-fluorouracil/leucovorin with oxaliplatin(FOLFOX) or XELOX. A treatment with trastuzumab is allowed in association.
  • Patient never treated by chemotherapy.
  • Patient with Performance Status under or equal to 2.
  • Patient with adequate hematopoietic, hepatic and cardiac functions according to the investigator.
  • Patient having read with the information note and having signed the informed consent.
  • Patient beneficiating from French health insurance cover.

Exclusion Criteria:

  • Patient with psychological state, geographical remote or social problems that contraindicated the participation into the study according to the investigator.
  • Patient that must be treated for a metastatic disease.
  • Patient not able to attend all study visits.
  • Patient not understanding French.
  • Patient who don't have a phone.
  • Vulnerable patient: pregnant or breast-feeding women, person deprived of freedom by an administrative or judicial decision, person older than 18 being the object of a legal protection measure or outside state to express their consent.

Sites / Locations

  • Centre Antoine Lacassagne
  • Polyclinique St Jean

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

A: Standard medical care

B: telephonic monitoring

Arm Description

Arm A: standard supervision and medical care during an adjuvant chemotherapy treatment in France

Arm B: telephonic monitoring during inter-treatment intervals + personalized medical care.

Outcomes

Primary Outcome Measures

emotional state (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation)
comparison of the 2 types of monitoring in terms of overall measure of emotional state (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation) of patients, with Profile of Mood States (POMS-f) questionnaire.

Secondary Outcome Measures

Evolution of emotional states scores
To compare 2 types of supervision in terms of: The difference between the overall scores on the POMS-f before the start of treatment, at each treatment and after 3 courses of treatment
toxicities
To compare 2 types of supervision in terms of proportion of patients with toxicity during treatment, and the maximum grade observed per patient
quality of life
To compare 2 types of supervision in terms of: The quality of life of the patient by the European Organization for Research and Treatment of Cancer Qulity of life questionnaire (EORTC QLQ-C30), before the start of treatment, during the 2nd cycle of chemotherapy and after three courses of treatment
anxiety
To compare 2 types of supervision in terms of: The level of anxiety assessed by the number of visits to psychologists, psychiatrists, the sub-score "Anxiety" obtained in the Hospital Anxiety and Depression State (HADS) questionnaire, the anxiolytics and antidepressants intakes
caregiver mood states
To compare 2 types of supervision in terms of: - The overall scores obtained by the caregiver on the POMS-f before, during and after 3 courses of treatment
patient satisfaction
To compare 2 types of supervision in terms of overall satisfaction scores obtained by the patient after 3 courses of treatment
relationship between psychosocial criteria and anxiety
To compare 2 types of supervision in terms of: - The relationship between the presence of psychosocial frailty criteria and the level of anxiety for patients in group B (number of visits to psychologists, psychiatrists; anxiolytics and antidepressants intake; HADS anxiety scores)

Full Information

First Posted
October 22, 2013
Last Updated
July 22, 2019
Sponsor
Centre Antoine Lacassagne
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1. Study Identification

Unique Protocol Identification Number
NCT01977053
Brief Title
Impact of a Telephonic Monitoring During Inter-treatment Intervals on Emotional State, Quality of Life and Toxicities, on Neo Adjuvant or Adjuvant Chemotherapy-treated Patients
Acronym
EMOTION
Official Title
Impact of a Telephonic Monitoring During Neo Adjuvant or Adjuvant Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
October 2018 (Actual)
Study Completion Date
December 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Antoine Lacassagne

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In health care, the phone has emerged as a clinical tool in its own right, especially for the development of psychological support to patients and that, in many pathologies. Its potential in the development of psycho-social support was quickly identified. However, to our knowledge, no prospective, randomized studies have evaluated the impact of a telephone call to both the anxiety and the management of side effects of neoadjuvant or adjuvant chemotherapy. The patient incomplete care by the hospital system and the general practitioner during chemotherapy, as well as the lack of information and poor preparation and / or management of side effects, are a source of distress and lead to a decrease quality of life for the patient and his family. We propose to determine on a population of 280 patients, the impact of two phone calls during 3 first inter-treatment intervals on the overall measure of mood states of the patient and his principal caregiver (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation). We will also study the gain in quality of life, on anxiety level, frequency and severity of toxicities, as well as emotional comfort of the procedure.
Detailed Description
Cancer is widely associated with the concept of psychological distress in a population of patients subject to numerous stressful events. Between 10 to 50% of patients with cancer and their families suffer from clinically significant psychological disorders. The existence of a broad continuum of manifestations of distress makes it difficult for clinical evaluation. Underestimated and misjudged, it is not always taken into account appropriately. However, these problems have a direct impact not only on the quality of life of patients but also on their ability to share decisions , adhere to treatment, and therefore to get the best care available for the treatment of their cancer. Interactions between the presence of psychopathological disorders, quality of life and treatment toxicities will be the focus of this study assessing the impact of telephonic monitoring (targeting clinical, psychological and social objectives) in patients with current chemotherapy. There are communication difficulties on the distress between the patient and the doctor, in part due to the gap between the perceptions of the patient and the caregiver. Indeed, many studies have highlighted the important differences existing between subjective psychosocial needs of the patient and the physician's ability to detect them. In particular, the study of Fallowfield on nearly 2300 medical consultations shows that only 29% of patients whose threshold of distress is clinically significant are identified by their doctors. Similarly, the synthesis carried out in 2005 by Thorne et al. reported the impact of failures of communication between clinicians and patients on the psychosocial experience of illness and treatment, symptom management, decision making and quality of life. Justification and research hypothesis In health care, the phone has emerged as a clinical tool in its own right, especially for the development of psychological support to patients and that, in many pathologies. Its potential in the development of psycho-social support was quickly identified. However, to our knowledge, no prospective, randomized studies have evaluated the impact of a telephone call to both the anxiety and the management of side effects of neoadjuvant or adjuvant chemotherapy. The patient incomplete care by the hospital system and the general practitioner during chemotherapy, as well as the lack of information and poor preparation and / or management of side effects, are a source of distress and lead to a decrease quality of life for the patient and his family. We propose to determine on a population of 280 patients, the impact of two phone calls during the first 3 inter-treatment intervals, the overall measure of mood states (anxiety, depression , confusion , anger , fatigue , vigor and interpersonal ) of the patient and his entourage . We also study the gain in quality of life, anxiety level, frequency and severity of toxicities, as well as emotional comfort of the procedure. We propose to determine on a population of 280 patients, the impact of two phone calls during the 3 first inter-treatment intervals on the overall measure of mood states of the patient and his principal caregiver (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation). We will also study the gain in quality of life, on anxiety level, frequency and severity of toxicities, as well as emotional comfort of the procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-metastatic Patients With Breast Cancer, Non-metastatic Patients With Colon Cancer, Non-metastatic Patients With Rectal Cancer, Patients Undergoing Adjuvant Chemotherapy
Keywords
breast cancer, colon cancer, rectal cancer, adjuvant chemotherapy, phone calls, emotional states, quality of life

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
274 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A: Standard medical care
Arm Type
No Intervention
Arm Description
Arm A: standard supervision and medical care during an adjuvant chemotherapy treatment in France
Arm Title
B: telephonic monitoring
Arm Type
Experimental
Arm Description
Arm B: telephonic monitoring during inter-treatment intervals + personalized medical care.
Intervention Type
Other
Intervention Name(s)
Clinical and psychosocial phone calls
Other Intervention Name(s)
medical care including social and psychological domains
Intervention Description
The standard medical supervision is defined as follows: Prescription of prophylactics medication (corticoid, antiemetic, cream, mouthwash, etc) at each cycle of chemotherapy. Nominative notebook containing details of chemotherapy administered and medical contacts. Consultations with psycho-oncologist or psychiatrist (if necessary). The intervention further comprises: nurse phone calls the 3rd and the 8th day of the first three cycles of treatment, and personalized medical care according to toxicities reported.
Primary Outcome Measure Information:
Title
emotional state (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation)
Description
comparison of the 2 types of monitoring in terms of overall measure of emotional state (anxiety, depression, confusion, angry, fatigue, force and interpersonal relation) of patients, with Profile of Mood States (POMS-f) questionnaire.
Time Frame
Change from baseline in POMS-f score at 6 weeks
Secondary Outcome Measure Information:
Title
Evolution of emotional states scores
Description
To compare 2 types of supervision in terms of: The difference between the overall scores on the POMS-f before the start of treatment, at each treatment and after 3 courses of treatment
Time Frame
Change from baseline in POMS-f score at 6 weeks; Change from baseline in POMS-f score at 9 weeks and Change from baseline in POMS-f score at 12 weeks
Title
toxicities
Description
To compare 2 types of supervision in terms of proportion of patients with toxicity during treatment, and the maximum grade observed per patient
Time Frame
up to 15 weeks
Title
quality of life
Description
To compare 2 types of supervision in terms of: The quality of life of the patient by the European Organization for Research and Treatment of Cancer Qulity of life questionnaire (EORTC QLQ-C30), before the start of treatment, during the 2nd cycle of chemotherapy and after three courses of treatment
Time Frame
Change from baseline in EORTC QLQ-C30 score at 6 weeks and Change from baseline in EORTC QLQ-C30 score at 12 weeks
Title
anxiety
Description
To compare 2 types of supervision in terms of: The level of anxiety assessed by the number of visits to psychologists, psychiatrists, the sub-score "Anxiety" obtained in the Hospital Anxiety and Depression State (HADS) questionnaire, the anxiolytics and antidepressants intakes
Time Frame
up to 15 weeks
Title
caregiver mood states
Description
To compare 2 types of supervision in terms of: - The overall scores obtained by the caregiver on the POMS-f before, during and after 3 courses of treatment
Time Frame
Change from baseline in POMS-f score at 6 weeks; Change from baseline in POMS-f score at 9 weeks and Change from baseline in POMS-f score at 12 weeks
Title
patient satisfaction
Description
To compare 2 types of supervision in terms of overall satisfaction scores obtained by the patient after 3 courses of treatment
Time Frame
up to 12 weeks
Title
relationship between psychosocial criteria and anxiety
Description
To compare 2 types of supervision in terms of: - The relationship between the presence of psychosocial frailty criteria and the level of anxiety for patients in group B (number of visits to psychologists, psychiatrists; anxiolytics and antidepressants intake; HADS anxiety scores)
Time Frame
up to 15 weeks
Other Pre-specified Outcome Measures:
Title
intervention cost
Description
To compare 2 types of supervision in terms of cost of the procedure (cost of consultations with psychologists, psychiatrists, cost of telephone calls)
Time Frame
up to 15 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient older than 18. Patient surgically-treated or no for non inflammatory breast cancer or for colon cancer or rectal cancer. Patient to be treated by neo-adjuvant or adjuvant chemotherapy by 5-fluorouracil, epirubicin and cyclophosphamide (FEC)-docetaxel, docetaxel-cyclophosphamide, 5-fluorouracil/leucovorin with oxaliplatin(FOLFOX) or XELOX. A treatment with trastuzumab is allowed in association. Patient never treated by chemotherapy. Patient with Performance Status under or equal to 2. Patient with adequate hematopoietic, hepatic and cardiac functions according to the investigator. Patient having read with the information note and having signed the informed consent. Patient beneficiating from French health insurance cover. Exclusion Criteria: Patient with psychological state, geographical remote or social problems that contraindicated the participation into the study according to the investigator. Patient that must be treated for a metastatic disease. Patient not able to attend all study visits. Patient not understanding French. Patient who don't have a phone. Vulnerable patient: pregnant or breast-feeding women, person deprived of freedom by an administrative or judicial decision, person older than 18 being the object of a legal protection measure or outside state to express their consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe FOLLANA, Dr.
Organizational Affiliation
Centre Antoine Lacassagne
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Antoine Lacassagne
City
Nice
State/Province
Cedex 2
ZIP/Postal Code
06189
Country
France
Facility Name
Polyclinique St Jean
City
Cagnes sur Mer
ZIP/Postal Code
06800
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
14996859
Citation
Ganz PA, Kwan L, Stanton AL, Krupnick JL, Rowland JH, Meyerowitz BE, Bower JE, Belin TR. Quality of life at the end of primary treatment of breast cancer: first results from the moving beyond cancer randomized trial. J Natl Cancer Inst. 2004 Mar 3;96(5):376-87. doi: 10.1093/jnci/djh060.
Results Reference
background
PubMed Identifier
17093275
Citation
Stanton AL. Psychosocial concerns and interventions for cancer survivors. J Clin Oncol. 2006 Nov 10;24(32):5132-7. doi: 10.1200/JCO.2006.06.8775.
Results Reference
background
PubMed Identifier
14581094
Citation
Carlson LE, Bultz BD. Cancer distress screening. Needs, models, and methods. J Psychosom Res. 2003 Nov;55(5):403-9. doi: 10.1016/s0022-3999(03)00514-2.
Results Reference
background
PubMed Identifier
12855257
Citation
Pitceathly C, Maguire P. The psychological impact of cancer on patients' partners and other key relatives: a review. Eur J Cancer. 2003 Jul;39(11):1517-24. doi: 10.1016/s0959-8049(03)00309-5.
Results Reference
background
PubMed Identifier
17623625
Citation
Vitek L, Rosenzweig MQ, Stollings S. Distress in patients with cancer: definition, assessment, and suggested interventions. Clin J Oncol Nurs. 2007 Jun;11(3):413-8. doi: 10.1188/07.CJON.413-418.
Results Reference
background

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Impact of a Telephonic Monitoring During Inter-treatment Intervals on Emotional State, Quality of Life and Toxicities, on Neo Adjuvant or Adjuvant Chemotherapy-treated Patients

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