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The Effect of Peer Support Program on the Sexual Quality of Life of Stoma Patients

Comparative Study of the Effect of Peer Support Program on the Sexual Quality of Life of Stoma Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190603043803N1
Enrollment
58
Registered
2019-08-18
Start date
2019-09-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Condition 1: Intestinal Ostomy (Ileostomy). Condition 2: Intestinal Ostomy(Colostomy). Surgical operation with formation of external stoma

Interventions

Intervention 1: The intervention of this study is using peer support program, which is organized as 4 group sessions to share common experiences of individuals with each other in order to increase the

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having a permanent Intestinal Stoma (Ileostomy and Colostomy) Pass at least 3 months from the surgery Being married Having complete alertness and consciousness Being fluent in persian

Exclusion criteria

Exclusion criteria: Patient dissatisfaction to participate in the study Having a history of participation in any related training program or research Having alcohol or drug addiction or taking medications that affect the sexual function Having advanced diseases of vital organs

Design outcomes

Primary

MeasureTime frame
One primary outcome variable is men's Sexual Quality of Life score in the men's Sexual Quality of Life questionnaire. Timepoint: Before the intervention(pretest), immediately and one month after the intervention(post tests). Method of measurement: The Men's Sexual Quality of Life Questionnaire is used. This questionnaire has 11 questions and it is scored based on a six-point Likert scale ranging from 1 to 6(quite disagree to quite agree). The range of questionnaire's score is from 11 to 66 and the higher score obtained from the questionnaire indicates the higher sexual quality of life.;Another primary outcome variable is women's Sexual Quality of Life score in the women's Sexual Quality of Life questionnaire. Timepoint: Before the intervention(pretest), immediately and one month after the intervention(post tests). Method of measurement: The Women's Sexual Quality of Life questionnaire is used. This questionnaire has 18 questions and is scored based on a six-point Likert scale ranging from 1 to 6 (strongly disagree to strongly agree). The range of questionnaire's score is from 18 to 108 and the higher the score obtained from the questionnaire, the higher the quality of sex life.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLadan Naseh

Esfahan University of Medical Sciences

naseh@nm.mui.ac.ir+98 31 3777 6981

Outcome results

None listed

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