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Systematic Symptom Identification With Disease Specific PROM to Assess Symptoms of Chronic GVHD in Outpatient Care in Patients Post HSCT

Systematic Symptom Identification With Disease Specific PROM to Assess Symptoms of Chronic GVHD in Outpatient Care in Patients Post HSCT - a Two Site Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04884204
Acronym
SIMPly-CARE
Enrollment
35
Registered
2021-05-12
Start date
2021-04-30
Completion date
2023-07-01
Last updated
2023-11-28

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

Conditions

GVHD, Chronic, Hematological Malignancy

Keywords

Lee Symptom Scale, Symptom management, Patient reported outcome

Brief summary

A two sited feasibility study to test the feasibility of systematic symptom identification with disease specific and clinically developed PROM (Lee Symptom Scale) longitudinally with a 12 month follow up in outpatient care in patients post HSCT to assess symptoms of chronic GVHD (n= 30).

Detailed description

A prospective, non-randomized, feasibility study examining a systematic approach to symptom management using PROMs with 12 months of follow up in hematological outpatient clinic

Interventions

BEHAVIORALLee Symptom Scala

Symptom identification and management with Lee Symptom Scale in follow up care

Sponsors

Novo Nordisk A/S
CollaboratorINDUSTRY
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Adults \> 18 years old * Approximately 3 months post HSCT (they will be included before HSCT, but the intervention will begin at 3 moths). * Patients included needs to be able to manage a computer to receive and respond to collect PRO data.

Exclusion criteria

* Patients who do not understand, read and speak Danish and/or have cognitive/psychiatric disorders not compatible with inclusion in a clinical study.

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rateRecruiment time frame: 12 monthsNumber of participants included from eligible participants
Adherence to interventionIntervention time frame: 12 months of follow upNumber of visits completed out of planned visits during intervention

Secondary

MeasureTime frameDescription
Quality of life measured by the European Organization for Research and Treatment of Cancer - quality of life questionnaire C30 (EORTC-QLQ-C30)12 months; at baseline (0 months), 6 and 12 monthsChange in quality of life measured by the European Organization for Research and Treatment of Cancer - quality of life questionnaire C30
Depression and Anxiety measured with the Hospital Anxiety and Depression Scale12 months; at baseline (0 months), 6 and 12 monthsChange in symptoms of depression and anxiety measured by the Hospital Anxiety Depression Scale
MD Andersons Symptom Inventory (MDASI)12 months; at baseline (0 months), 6 and 12 monthsChange in symptom burden measured by the scale M.D. Andersons Symptom Inventory
HM-PRO questionaire developed by the 'Scientific Working Group for QoL and Symptoms,' within the European Hematology Association12 months; at baseline (0 months), 3, 6, 9 and 12 monthsChange in HM-PRO developed by The 'Scientific Working Group for QoL and Symptoms,' within the European Hematology Association

Other

MeasureTime frameDescription
Referrals to municipality12 months of follow up from date of transplantationNumber of referrals to rehabilitation in the municipality within the study period
DiagnoseAt baselineDiagnose at baseline
Number of telephone contacts to Dept. of Hematology12 months of follow up from date of transplantationNumber of telephone contacts to Dept. of Hematology within the study period
Infections treated with antibiotics12 months of follow up from date of transplantationNumber of infections treated with antibiotics within the study period
MedicationAt baselineMedication at baseline
Immunosuppresive drugs12 months of follow up from date of transplantationImmunosuppresive drugs the participants receive after transplantation (within the study period)
Hospitalization12 months of follow up from date of transplantationPeriods with hospitalizations within the study period
Referrals to other hospital departments12 months of follow up from date of transplantationNumber of referrals to other hospital departments within the study period
Referrals to general practitioner12 months of follow up from date of transplantationNumber referrals to general practitioner within the study period

Countries

Denmark

Outcome results

None listed

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