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Adherence to Treatment in Hemophilia (ADHERENCE)

A

ANA TORRES-ORTUÑO

Status

Unknown

Conditions

Haemophilia

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02191436
ADHE (Other Identifier)
ADHERENCE

Details and patient eligibility

About

Psychosocial factors and adherence to treatment in patients with hemophilia. A multicenter study. Multicenter cross sectional study of patients with hemophilia and their families

Full description

Research project whose main objective is to assess adherence and major psychosocial issues affecting patients with hemophilia and their families treated at the Hematology and hemotherapy Services Clinical Hospital Universitario Virgen de la Arrixaca of Murcia and the University Hospital Carlos Haya, Malaga.

The data obtained in this project will identify those psychosocial aspects affecting patients and their families about the disease, its evolution and treatment of it. They will use different psychosocial questionnaires based on scientific evidence and the reliability of these, as well as its specific design for hemophilia patients. The main characteristics of the study are:

  • Descriptive study of adherence to treatment of pediatric patients, adolescents and adults with hemophilia.
  • Descriptive study of family functioning, perceived stress, anxiety and quality of life in parents of children with hemophilia under 14 years and adolescents with hemophilia, depending on the administered medical treatment, clinical and musculoskeletal patient situation.
  • Descriptive study of illness behavior or perception of illness, perceived stress, anxiety, quality of life and coping strategies of young adults with hemophilia, depending on the medical treatment administered, and skeletal muscle clinical situation of the patient.
  • Validation of psychosocial assessment tools in patients with hemophilia and their families.

Enrollment

200 estimated patients

Sex

Male

Ages

6 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with hemophilia A or B
  • Patients followed at the Hematology Department of the hospitals included in the study
  • Patients without cognitive disorders

Exclusion criteria

  • Patients with other congenital coaguopatías
  • Patients with more than 2 years without going to review your hospital
  • Patients from other provinces of Spain

Trial design

200 participants in 1 patient group

Patients with haemophilia
Description:
Hemophilia patients (children, youth and adults) and parents of children with hemophilia under 18

Trial contacts and locations

1

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Central trial contact

ANA TORRES-ORTUÑO, PhD; RUBÉN CUESTA-BARRIUSO, PhD

Data sourced from clinicaltrials.gov

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