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Home Care in Allogeneic Haematopoietic Stem Cell Transplantation

Impact of Home Care for Recipients of Allogeneic Haematopoietic Stem Cell Transplantation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04707417
Enrollment
16
Registered
2021-01-13
Start date
2022-02-01
Completion date
2023-08-01
Last updated
2023-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

GVH - Graft Versus Host Reaction, Quality of Life, Stem Cell Transplant Complications

Brief summary

Mixed methods study with focus groups interviews and a prospective observational cohort study aimed to investigate the impact of advanced home care on transplant specific outcomes and quality of life in recipients of allogeneic hematopoietic stem cell transplantation

Detailed description

Study of advanced home care after allogeneic haematopoietic stem cell transplantation (allo-HSCT). The main objective is to investigate the impact of home care on transplant specific variables and quality of life (QoL). The main hypothesis is that home care patients will home care patients will have significantly better measured QoL than patients receiving in-hospital care during the first 6 weeks after allo-HSCT. The study will be conducted as part of routine care at the departement of haematology, Oslo University Hospital. There are qualitative and quantitative aspects to the study. The qualitative part involves focus groups interviews with patients that have been treated with allo-HSCT and have recieved home care and their caregivers. In the prospective observational cohort study data will be collected to compare patients receiving home care and patients treated in-hospital (control group). Patients in both groups wil answer the questionnaire EORTC QLQ-C30 once weekly for 6 weeks. In addition transplant- and treatment-specific variables will be collected and compares between the groups.

Interventions

Advanced home care

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Consent competency and written informed consent to participation * Age ≥18 * Understanding and willing to comply with written and oral instructions in Norwegian * Planned treatment with allo-HSCT * ECOG performance status 0-2 * Caregiver (age ≥18) present 24 hours a day during the aplastic phase * Travelling distance from residence to the hospital must be less than one hour.

Exclusion criteria

* Not meeting inclusion criteria * Uncontrolled infection or other medical condtion unsuitable for out patient care

Design outcomes

Primary

MeasureTime frameDescription
GRFS1 yearGvHD-free, relapse-free survival
QoL6 weeksQuality of Life

Secondary

MeasureTime frameDescription
GvHD1 yearGraft versus host disease
TRM1 yearTransplant related mortality
Infection1 yearBacteriemia and invasive fungal disease

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026