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Online Symptom Questionnaires for Older Adults With Acute Leukemia

Tests online questionnaires on how patients feel, in older adults with acute leukemia.

Plain-language title generated from the registry record
Registry title: Digital Patient-Reported Assessment in Older Adults With Acute Leukemia

Key facts

Where
Oviedo, SpainSee the site

Where in Spain

  • Hospital Universitario Central de Asturias (HUCA)Oviedo, SpainNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Fundación para la Investigación Biosanitaria del Principado de Asturias
Trial code
NCT07597590
Record updated
7 October 2026
Original description
This pilot study will evaluate the feasibility of implementing a structured digital patient-reported assessment pathway in adults aged 65 years or older with acute leukemia at Hospital Universitario Central de Asturias, Oviedo, Spain. Participants will complete the EORTC QLQ-C30 and FACT-Leu remotely after the baseline visit and repeat the digital assessment 8-12 weeks after individual activation of the MiAsturSalud/SESPA digital pathway. The primary outcome will be the proportion of participants answering at least 80% of the items in the baseline digital questionnaire battery within 7 days after the baseline visit. Secondary outcomes will be caregiver assistance requirement, non-completion of the planned digital follow-up assessment, and elapsed baseline questionnaire completion time. During this feasibility study, participants will not concurrently receive the broader project's home-monitoring and clinical-alert intervention. The questionnaire pathway will not generate automated clinical alerts. Usual clinical care will continue. The study is not designed to establish clinical efficacy.Read full original descriptionShow less

Feasibility of a Structured Digital Patient-Reported Assessment Pathway in Older Adults With Acute Leukemia: A Prospective Single-Center Pilot Study

This pilot study will evaluate the feasibility of implementing a structured digital patient-reported assessment pathway in adults aged 65 years or older with acute leukemia at Hospital Universitario Central de Asturias, Oviedo, Spain. Participants will complete the EORTC QLQ-C30 and FACT-Leu remotely after the baseline visit and repeat the digital assessment 8-12 weeks after individual activation of the MiAsturSalud/SESPA digital pathway. The primary outcome will be the proportion of participants answering at least 80% of the items in the baseline digital questionnaire battery within 7 days after the baseline visit. Secondary outcomes will be caregiver assistance requirement, non-completion of the planned digital follow-up assessment, and elapsed baseline questionnaire completion time. During this feasibility study, participants will not concurrently receive the broader project's home-monitoring and clinical-alert intervention. The questionnaire pathway will not generate automated clinical alerts. Usual clinical care will continue. The study is not designed to establish clinical efficacy.

Inclusion: Age 65 years or older; Confirmed diagnosis of acute leukemia of myeloid or lymphoid origin; Active ambulatory follow-up in the Hematology Service at Hospital Universitario Central de Asturias; Ability to understand the questionnaires and provide their own responses, independently or with practical assistance from a caregiver; Access to a compatible internet-enabled digital device, either personally or through a caregiver; Provision of written informed consent.

Exclusion: Cognitive impairment that, in the treating hematologist's clinical judgment, prevents the participant from understanding the questionnaires or providing their own responses, despite permitted practical assistance from a caregiver; Clinical condition that, in the treating hematologist's judgment, precludes completion of the study procedures; Persistent inability to access or use the MiAsturSalud/SESPA platform despite reasonable technical support.

ClinicalTrials.gov NCT07597590