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Investigating The Effect of The Educational-Supportive Program on The Quality of Recovery and Satisfaction with The Quality of Patient Care

Investigating The Effect of The Educational-Supportive Program on The Quality of Recovery and Satisfaction with The Quality of Care of Patients Undergoing Thoracotomy due to Hydatid Cyst.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240407061438N1
Enrollment
70
Registered
2024-06-09
Start date
2024-06-09
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Hydatid cyst disease. Echinococcus granulosus infection of lung

Interventions

Intervention 1: Intervention group: For the people in the intervention group, an educational-support program will be implemented from the beginning of their hospitalization and the day before the surg

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Definitive Diagnosis of Hydatid cyst Candidate for Thoracotomy Surgery Due to Hydatid Cyst Informed Consent of The Patient to Participate in The Study Full Consciousness and Being Aware of Place and Time Age between 18-65 years Not Having Hearing Problems (sitting fully Despite The Use of Assistive Devices) and Vision (Ability to Read a Newspaper at a Distance of 30cm with Glasses) Ability to Read and Write No History of Mental Disorders Need Surgery Not Having Employment as a Member of the Treatment Staff No Underlying Disease (Asthma, Empyema, Lung Cancer, Tuberculosis, etc.)

Exclusion criteria

Exclusion criteria: Death of The Patient The Patient's GCS Drops so that he/she is Unable to Communicate Unwillingness to Continue Cooperation in Conducting Research at any Stage Participation in Similar Training Courses Previous History of Heart and Lung Surgery

Design outcomes

Primary

MeasureTime frame
The Quality of Patients' Recovery. Timepoint: Measuring The Quality of Recovery of Patients on The First Day After Surgery, 3 Days After Surgery and The Fifth Day After Surgery. Method of measurement: Recovery Quality Questionnaire (QOR-40).;Satisfaction with The Quality of Patient Care. Timepoint: Measuring Satisfaction with The Quality of Patient Care at The End of The Fifth Day of Hospitalization. Method of measurement: Patient Satisfaction Wolf Instrument (PSI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Haji Abadi

Mashhad University of Medical Sciences

Hajiabadif@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026