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Investigating the effect of clinical orientation teaching on anxiety, pain and satisfaction of patients candidating for endoscopy

Investigating the effect of clinical orientation teaching on anxiety, pain and satisfaction of patients candidating for endoscopy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171002036498N4
Enrollment
60
Registered
2021-03-17
Start date
2021-04-21
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Gastrointestinal patients. Gastrointestinal hemorrhage, unspecified

Interventions

Intervention 1: Intervention group: The intervention group receives in addition to routine ward training, clinical familiarization intervention with endoscopic procedure. Clinical familiarization is

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Prescribed endoscopy No history of endoscopy Non-emergency endoscopy No cognitive problems No physical disability Do not be deaf No visual impairment No history of mental illness Do not have severe pain due to other diseases (cancer, etc.) Ability to speak Persian

Exclusion criteria

Exclusion criteria: Uncooperative patient to continue The patient becomes ill or has a complication Use more sedatives than usual

Design outcomes

Primary

MeasureTime frame
Anxiety: The score that patients receive from the Spielberger situational questionnaire This numerical score is higher than 43. Timepoint: Before and after the intervention. Method of measurement: Spielberger Anxiety Scale.;Satisfaction: The patient's feeling is about the performance of the treatment team, the condition of the disease and the diagnostic-therapeutic methods. Timepoint: Before and after the intervention. Method of measurement: Satisfaction Questionnaire.

Secondary

MeasureTime frame
Unpleasant sensation and emotional experience. Timepoint: After the intervention. Method of measurement: Visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Akbari

Rafsanjan University of Medical Sciences

iccn87@gmail.com+98 34 3426 2818

Outcome results

None listed

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