Skip to content

Effect of training on Anxiety, stress, pain

Effect of training on Anxiety, stress, pain management and some postoperative complications in abdominal surgery patients referring to Ali ibn Abitaleb Hospital in Rafsanjan in 2019

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180729040630N1
Enrollment
200
Registered
2019-02-18
Start date
2019-03-21
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Condition 1: Abdominal pain. Condition 2: anxiety. Condition 3: Stress. Abdominal and pelvic pain Other anxiety disorders Stress, not elsewhere classified

Interventions

Intervention 1: Intervention group: Training by a doctor (Training by physician  Individually, one session will be performed for 30 minutes 48 hours before surgery. Training includes providing compreh

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Criteria for entering the study: Age between 18 and 75 years Patient with criteria for performing elective surgery in the abdomen To be hospitalized for up to 46 hours after surgery. Ability to understand and speak Persian Interested in participating in the study The absence of mental illness recorded in the case Able to communicate and understand the questionnaire Non-drug addiction and other narcotic drugs No history of chronic pain

Exclusion criteria

Exclusion criteria: Exit criteria: Unwillingness of patients to continue reading There is no problem as long as the patient is unable to continue studying Return to the operating room Confusion during the postoperative period Admission to the Intensive Care Unit Participate in another clinical trial at the same time Any factor that causes the patient to get out of reach 48 hours (lack of cooperation, early clearance, and personal satisfaction).

Design outcomes

Primary

MeasureTime frame
Pain management. Timepoint: After the intervention. Method of measurement: Revised American Pain Society Patient Outcome Questionnaire.;Anxiety. Timepoint: Before and after intervention. Method of measurement: state-trait anxiety inventory.;Emotional preoperative stress. Timepoint: Before intervention. Method of measurement: brief measure of emotional preoperative stress.

Secondary

MeasureTime frame
Postoperative complications. Timepoint: after intervention. Method of measurement: Report the type of postoperative complications.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ali Zakeri

Rafsanjan University of Medical Sciences

mazakeri@rums.ac.ir+98 34342316

Outcome results

None listed

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