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Effect of Artificial Intelligence-Based Self-Care Educational Intervention on Self-Efficacy and Health Literacy

Effect of Artificial Intelligence-Based Self-Care Educational Intervention on Self-Efficacy and Health Literacy in Women with Pelvic Inflammatory Disease (PID): A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200107046044N8
Enrollment
88
Registered
2025-11-26
Start date
2025-12-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Pelvic Inflammatory Disease (PID). Female pelvic inflammatory disease, unspecified

Interventions

Intervention 1: Intervention group: In this group, the interventions will be conducted according to the protocol, briefly outlined over eight sessions as follows:Session 1: Introduction of participant

Sponsors

Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: The ability to communicate and respond to questions Age between 18 and 40 years Willingness to participate in the study and signing the informed consent form Definitive diagnosis of Pelvic Inflammatory Disease (PID) by the relevant specialist physician Concurrent attainment of a score of 51 or below on the Sherer et al.'s General Self-Efficacy Scale-17 (SGSES-17) and a score of 50 (equivalent to a raw score of 27) or below on the Health Literacy Instrument for Adults-Short Form (HELIA-SF) No use of psychoactive medications or any other drugs that may adversely affect concentration and learning. No prior training or participation in studies similar to the current research within the past 6 months

Exclusion criteria

Exclusion criteria: Lack of willingness to participate in the study The presence of severe psychological disorders (such as severe depression or severe anxiety) that require specialized treatment. A recent history of pelvic surgery (within the past approximately three months) that may destabilize the individual’s health status. Use of sedatives, anxiolytics, or antidepressants prior to the intervention Exacerbation of disease symptoms and the need for urgent medical treatment Pregnancy during the study period The presence of severe immune system disorders or concurrent active infections that may affect the treatment process.

Design outcomes

Primary

MeasureTime frame
The Self-Efficacy score is derived from the Sherer et al.'s General Self-Efficacy Scale-17 (SGSES-17). Timepoint: Before the implementation of the interventions and one month after the completion of the interventions. Method of measurement: Sherer et al.'s General Self-Efficacy Scale-17 (SGSES-17).;The Health Literacy score is derived from the Health Literacy Instrument for Adults-Short Form (HELIA-SF). Timepoint: Before the implementation of the interventions and one month after the completion of the interventions. Method of measurement: Health Literacy Instrument for Adults-Short Form (HELIA-SF).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadSajjad Mousavi

Ahvaz University of Medical Sciences

sajjad.mousavi2512@gmail.com+98 61 5242 1065

Outcome results

None listed

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