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Comparing the effect of GUIDED IMAGERY and CRYOTHERAPY(cold compress) on post operative pain severity and vital signs among laparoscopic cholecystectomy inpatients in Teaching Hospitals

Comparing the effect of GUIDED IMAGERY and CRYOTHERAPY(cold compress) on post operative pain severity and vital signs among laparoscopic cholecystectomy inpatients in Teaching Hospitals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230723058896N1
Enrollment
93
Registered
2023-09-09
Start date
2023-09-11
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Laparoscopic cholecystectomy. Calculus of gallbladder with acute cholecystitis with obstruction

Interventions

Intervention 1: Intervention group: In order to guided imagery , 20-minute voices or images will be used for this purpose under the supervision of a specialist consultant, according to the person's pr

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Candidate for laparoscopic cholecystectomy surgery Satisfaction and willingness to participate in the research Age between 20-60 years old Alertness after the operation the disappearance of the effects of anesthetic drugs before the start of the intervention Ability to use numerical scale of pain intensity Having pain with a score greater than 3 No impairment in speech, hearing, vision and communication Ability to speak Persian or Turkish Do not have heart surgery or any cardiovascular disorder Do not have a disease related to the prohibition of the use of cold, such as Raynaud's syndrome No history of nerve diseases (neuropathy, muscle stiffness and poor blood circulation) Any confirmed mental illness

Exclusion criteria

Exclusion criteria: Unwillingness to participate and continue studying Occurrence of physical problems and inability to continue the plan Discharge of the patient by personal consent or death of the patient Performing any procedure outside the routine schedule Use of PCA pump

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: Before the start of the intervention (zero time) - 15-30-45-60 minutes. Method of measurement: Visual analogue scale questionnaire.;Vital signs. Timepoint: 15-30-45-60 minutes. Method of measurement: Portable monitoring device and thermometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShasaddin Shamsi

Oroumia University of Medical Sciences

shamsi_sh@umsu.ac.ir+98 44 3275 4961

Outcome results

None listed

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