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Effect of discharge planning upon heart valve replacement patient.

Effect of designed discharge plan on self efficacy, anxiety and length of post -operative hospital staying in people with heart valve replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016092312452N4
Enrollment
70
Registered
2016-10-11
Start date
2016-07-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Heart valve replacement. Other heart disorders in diseases classified elsewhere

Interventions

this study is a clinical trial Two groups and three-stage that 70 of patients candidate for open heart valve replacement are selected by randomaly sampling and after take consent.the patients of contr
Behavior

Sponsors

Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-The desire to participate in the study; 2- Being candidate for the open heart surgery; 3- Patient or their families have ability to read; 4- No need for urgent surgery; 5- First time open heart surgery; 6- Patients have not anxiety disorders or cognitive problems; 7- Patients have access to the phone; 8- Age between 18 and 80 years old. Exclusion criteria: 1-The patient's unwillingness to continue to participate in the study; 2- Died during the operation or after it; 3- Mechanical ventilation more than 95 hours or need to tracheostomy after surgery; 4- Need to dialysis related to renal failure before or after surgery; 5- Stroke before or after surgery; 6- Any gastrointestinal adverse event that requires treatment or surgical interventions such gastrointestinal bleeding or ileus after surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Self efficacy. Timepoint: Before interventin, 1 month after intervention, 3 months after intervention. Method of measurement: Sullivan questionnaire.;Anxiety. Timepoint: Before interventin, 1 month after intervention, 3 months after intervention. Method of measurement: Spielberger questionnaire.;Length of hospital staying. Timepoint: Length of post -operative hospital staying. Method of measurement: Medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEsmeial Shafiei Ashegh Abadi

Shahrekord University of Medical Sciences

esmeial68@gmail.com+98 38 3333 5654

Outcome results

None listed

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