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mHealth to Improve the Experience, Adherence to Drug Treatment and Positive Mental Health

H

Hospital Clinic of Barcelona

Status

Enrolling

Conditions

Fracture of Femur

Treatments

Other: Patient Experience
Other: Training in the use of MyPlan Aplication
Other: Pharmacological education

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT05669040
Intervention EFE

Details and patient eligibility

About

The present study aims to evaluate the effectiveness of a pharmacological nursing educational intervention (EFE) with "Myplan Aplication" about the patient's experience, adherence to pharmacological treatment, and positive mental health of patients with femur fracture.

Full description

Once the informed consent has been obtained, the investigators will explain to the patient the pharmacological treatment with the support of an aplication (what it is for, how the medication should be taken, possible adverse effects), also the investigators will share time with the patient during the 4 face-to-face training sessions. The investigators will accompany during their hospital stay, offering to pacients telematic support upon discharge with the treatment and until the end of the study. This is a quasi-experimental non-randomized study with 3 phases of data collection. Possible adverse reactions, if any, will be recorded.

Enrollment

278 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of femur fracture
  • knowledge of the Spanish language
  • 24-hour admission to the traumatology unit
  • level of consciousness on the Glasgow scale of 15
  • have access to a mobile device
  • ability to participate in the pilot study
  • be able to provide written informed consent or obtain consent from a legal representative.

Exclusion criteria

  • presence of psychological pathologies or cognitive impairment
  • isolation in hospital admission

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

278 participants in 3 patient groups

Patient experience
Active Comparator group
Treatment:
Other: Training in the use of MyPlan Aplication
Other: Patient Experience
Other: Pharmacological education
Adherence to drug treatment
Active Comparator group
Treatment:
Other: Training in the use of MyPlan Aplication
Other: Pharmacological education
Positive mental health
Active Comparator group
Treatment:
Other: Patient Experience

Trial contacts and locations

1

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Central trial contact

Gemma Marcos Anton; Montserrat Puig LLobet

Data sourced from clinicaltrials.gov

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