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Feasiblity and Safety of Home-based Intensive Chemotherapy

Primary Purpose

Acute Leukemia

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Home-based chemotherapy
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Acute Leukemia

Eligibility Criteria

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

Inclusion Criteria:

Participants 18 years or older were included within the first 28 days from diagnosis with AML or high-risk MDS if intensive chemotherapy treatment was planned.

Exclusion Criteria:

Patients were excluded if they did not understand, read and speak Danish, suffered from a severe illness requiring hospitalization if they had an unstable medical disease or any cognitive/psychiatric disorders. During the intervention, participants were withdrawn if hospitalized in an intensive care unit for more than two weeks, if they had a psychological condition (delirium or severe depression), or in case of transition to terminal care or if deceased. Moreover, participants were censored if they relapsed or transitioned to hematopoietic stem cell transplantation (HSCT).

Sites / Locations

  • Aalborg University Hospital
  • Aarhus University Hospital
  • Herlev Hospital
  • Odense University Hospital
  • Sjællandsuniversitetshospital Roskilde
  • Rigshospitalet

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Feasiblity and Safety

Arm Description

All eligible patients will be assigned to this arm

Outcomes

Primary Outcome Measures

Recruitment rate
Number of participants included from eligible patients
Adherence to intervention
Number of weeks completed out of planned weeks of intervention
Hospital admissions
Data will be collected from medical charts
Infections (days)
Data will be collected from medical charts
Infections (type)
Data will be collected from medical charts
Number of days home during treatment
Data will be collected from medical charts
Number of contacts to hospital during treatment
Data will be collected from medical charts
Number of removed CVK
Data will be collected from medical charts

Secondary Outcome Measures

Psychological wellbeing
Measured using the Hospital Anxiety and Depression Scale (HADS)
Quality of Life in participants
Measured with the Functional Assessment of Cancer Therapy - Leukemia (FACT-LEU)
Quality of Life in participants
Measured with the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)

Full Information

First Posted
May 22, 2021
Last Updated
May 22, 2021
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT04904211
Brief Title
Feasiblity and Safety of Home-based Intensive Chemotherapy
Official Title
A National Danish Proof of Concept on Feasiblity and Safety of Home-based Intensive Chemotherapy in Patients With Acute Leukemia.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
January 2017 (Actual)
Primary Completion Date
September 2020 (Actual)
Study Completion Date
September 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
a multicenter single-arm feasibility and safety study of home-based intensive chemotherapy in patients with newly diagnosed acute myeloid leukemia and their quality of life and psychological wellbeing. This national study included patients from six sites in Denmark who received intensive chemotherapy on programmed CADD Solis infusion pumps through a central venous catheter and were also managed as outpatients during treatment-induced pancytopenia.
Detailed Description
This national single-arm feasibility cohort study was conducted at six hematology departments at six university hospitals in Denmark: Copenhagen University Hospital, Rigshospitalet; Herlev/Gentofte Hospital; Zealand University Hospital, Roskilde; Odense University Hospital; Aarhus University Hospital, and Aalborg University Hospital. The project nurse at each site approached and recruited participants from October 2017 to August 2020. The participants were explicitly evaluated for their ability to manage their symptoms, administer oral medication, eat and drink sufficiently, and practice good personal hygiene. Eligible participants received oral and written information and provided written informed consent before inclusion. Included participants received intensive chemotherapy treatment on a CADD pump through their CVC. The CADD pump is unique because it is portable, carried in a small bag or backpack, and applicable for home-based treatment due to its intuitive and user-friendly interface. A patient educational program based on strategic patient involvement was integrated into supportive care practice during induction treatment at each hematology department. The program included guidance and training to the patient and/or their primary caregiver in managing the care of their CVC including drawing blood samples, how to use a positive expiratory pressure whistle, functionality of the infusion pump, how to manage and react on pump alarm, and precautions when receiving treatment while being home. The participants could contact the hematological department from where they received their treatment 24 hours a day by telephone. They were instructed to contact their respective department immediately if fever (>38.0 Celcius) or any pump report alarm occurred. The nurses would then guide the participant to solve the problem from home or recommend they seek help at the department to solve the problem or get evaluated by a doctor. Adverse events were categorized into non-serious adverse events and serious adverse events. Non-serious adverse events were any pump infusion alarms that could not be solved by phone and required a visit to the hospital. Serious adverse events were any adverse reactions during treatment at home, which resulted in the following outcomes: death or septic shock.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Leukemia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
104 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Feasiblity and Safety
Arm Type
Experimental
Arm Description
All eligible patients will be assigned to this arm
Intervention Type
Other
Intervention Name(s)
Home-based chemotherapy
Intervention Description
To investigate the feasibility and safety of home-based intensive chemotherapy in patients with newly diagnosed acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS). Furthermore, we examined the quality of life (QOL) and psychological wellbeing while receiving induction and consolidation chemotherapy at home.
Primary Outcome Measure Information:
Title
Recruitment rate
Description
Number of participants included from eligible patients
Time Frame
up to 3 years
Title
Adherence to intervention
Description
Number of weeks completed out of planned weeks of intervention
Time Frame
Up to 24 weeks
Title
Hospital admissions
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Title
Infections (days)
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Title
Infections (type)
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Title
Number of days home during treatment
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Title
Number of contacts to hospital during treatment
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Title
Number of removed CVK
Description
Data will be collected from medical charts
Time Frame
Up to 24 weeks
Secondary Outcome Measure Information:
Title
Psychological wellbeing
Description
Measured using the Hospital Anxiety and Depression Scale (HADS)
Time Frame
Change measures (baseline, 12 weeks, 24 and 36 weeks)
Title
Quality of Life in participants
Description
Measured with the Functional Assessment of Cancer Therapy - Leukemia (FACT-LEU)
Time Frame
Change measures (baseline, 12 weeks, 24 and 36 weeks)
Title
Quality of Life in participants
Description
Measured with the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)
Time Frame
Change measures (baseline, 12 weeks, 24 and 36 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants 18 years or older were included within the first 28 days from diagnosis with AML or high-risk MDS if intensive chemotherapy treatment was planned. Exclusion Criteria: Patients were excluded if they did not understand, read and speak Danish, suffered from a severe illness requiring hospitalization if they had an unstable medical disease or any cognitive/psychiatric disorders. During the intervention, participants were withdrawn if hospitalized in an intensive care unit for more than two weeks, if they had a psychological condition (delirium or severe depression), or in case of transition to terminal care or if deceased. Moreover, participants were censored if they relapsed or transitioned to hematopoietic stem cell transplantation (HSCT).
Facility Information:
Facility Name
Aalborg University Hospital
City
Aalborg
Country
Denmark
Facility Name
Aarhus University Hospital
City
Aarhus
Country
Denmark
Facility Name
Herlev Hospital
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
Facility Name
Odense University Hospital
City
Odense
Country
Denmark
Facility Name
Sjællandsuniversitetshospital Roskilde
City
Roskilde
ZIP/Postal Code
4000
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
State/Province
Østerbro
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34839055
Citation
Norskov KH, Fridthjof K, Kampmann P, Dunweber A, Andersen CL, Renaberg T, Schollkopf C, Ahmad SA, Schou K, Jensen CF, Moller P, Lundholm BW, Marcher C, Jepsen L, Orntoft AK, Ommen HB, Andersen L, Behrentzs A, Hasselgren CF, Severinsen M, Grand MK, Jarden M, Moller T, Kjeldsen L. A national Danish proof of concept on feasibility and safety of home -based intensive chemotherapy in patients with acute myeloid leukemia. Leuk Res. 2022 Jan;112:106756. doi: 10.1016/j.leukres.2021.106756. Epub 2021 Nov 22.
Results Reference
derived

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Feasiblity and Safety of Home-based Intensive Chemotherapy

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