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The effect of the social support program on the quality of life and perceived social support of women undergoing hysterectomy

Investigating the effect of the social support program on the quality of life and perceived social support of women undergoing hysterectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181207041873N4
Enrollment
86
Registered
2025-07-30
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

The effect of a multifaceted social support program on the quality of life and perceived social support of women undergoig hysterectomy.

Interventions

This quasi-experimental clinical trial will be conducted on 86 patients undergoing abdominal hysterectomy. To prevent data contamination between the two groups, participants will be alternated one wee

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Iranian nationality Marital Status: Married Language: Persian Minimum literacy required to complete the questionnaires Indication for abdominal hysterectomy with the approval of a gynecologist

Exclusion criteria

Exclusion criteria: Use of drugs and medications related to mental disorders History of current or previous psychiatric disorders, as reported by the research units Hysterectomy performed due to cancer or complications following vaginal delivery or cesarean section

Design outcomes

Primary

MeasureTime frame
Examining the differences, or the absence of differences, in perceived social support among women undergoing abdominal hysterectomy. Timepoint: Before the intervention and eight weeks after the completion of the training sessions. Method of measurement: Multidimensional Perceived Social Support Scale (MSPSS).

Secondary

MeasureTime frame
Difference or no difference in quality of life in women undergoing abdominal hysterectomy. Timepoint: Before the intervention and eight weeks after the completion of the training sessions. Method of measurement: WHO Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyede Batool Hasanpoor-Azghady

Iran University of Medical Sciences

hasanpoor.sb@iums.ac.ir+98 21 2288 5394

Outcome results

None listed

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