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The effect of feedback-based self-care training on pain intensity and sleep quality in patients with endometriosis

The effect of feedback-based self-care training on pain intensity and sleep quality in patients with endometriosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200521047534N3
Enrollment
60
Registered
2024-12-23
Start date
2024-12-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Endometriosis. Endometriosis

Interventions

Intervention 1: Intervention group: Intervention group: The research is conducted in four stages. the first stage
Completion of demographic questionnaire, visual pain scale and Pittsburgh sleep quality index as self-report by samples. the second stage
Conducting intervention and holding training sessions. The process of training sessions for each person includes two training sessions in two days with an interval of three to four days in such a way
About the nature of endometriosis disease (causes, stages, side effects and treatment) and usual training according to the doctor's recommendation (treatment regimen), self-care (purpose of self-care
Telephone follow-ups during four weeks are to ensure the continuation of self-care, guidance, clarification of ambiguities and answers to the samples' questions. The fourth stage will be re-completion

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Reading and writing literacy Able to understand Persian language Sleep disorder (score above 6 according to the questionnaire) Diagnosis of stage II, I or III endometriosis in the last 5 years Continuous pelvic pain with intensity between 3 and 10 on a 10-point numerical scale

Exclusion criteria

Exclusion criteria: Psychological diseases Being employed in the treatment system chronic diseases (cardiovascular disease, asthma, cancer) Taking psychotropic drugs Reluctance to participate in training sessions (not attending even one training session) The use of various complementary medicine methods during the previous three months Taking sleeping pills and sedatives Physical problems that prevent a person from moving

Design outcomes

Primary

MeasureTime frame
Pain level using Visual Analog scale (VAS). Timepoint: The Level of pain before and 2 monthly cycles after of the intervention will be investigated and recorded using the visual analog scale (VAS) in both intervention and control groups. Method of measurement: visual analog scale.

Secondary

MeasureTime frame
Sleep quality score using the Pittsburgh Sleep Quality Questionnaire (PSQI). Timepoint: The amount of sleep quality before and 2 monthly cycles after of the intervention will be checked and recorded in both intervention and control groups. Method of measurement: Pittsburgh Sleep Quality Questionnaire (PSQI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Seifi

Shiraz University of Medical Sciences

z.seifi2010@yahoo.com+98 71 3647 4254

Outcome results

None listed

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