The effect of Psycho-spiritual approach in women with type 2 diabetes

Investigating the effect of of Psycho-spiritual approach in improving sexual performance, sleep quality and depression in women with type 2 diabetes: randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220704055367N2

Enrollment

Registered

2022-09-10

Start date

2022-10-22

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

Type 2 diabetes. Diabetes mellitus due to underlying condition

Interventions

Intervention 1: Intervention group: It will be formed in the intervention group in order to create group coordination in WhatsApp. Group meetings will be held in groups of 30 people. In order to imple

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Married women aged 18 to 45 with type 2 diabetes Diagnosed with diabetes by a doctor and at least one year has passed since the diagnosis of diabetes Being interested in participating in the study Not having mental incompetence, including any kind of mental or cognitive disorder that prevents participation in the interaction process, adherence to the program, or giving informed consent to participate in this study Having Persian dialect

Exclusion criteria

Exclusion criteria: Participating in unusual educational programs or similar research while conducting research Inability to continue participating in the study for any reason (need for special care, immigration, death) Failure to participate in all meetings

Design outcomes

Primary

Measure	Time frame
Sexual performance scores on Female Sexual Function Index. Timepoint: Measurement of women's sexual performance scores at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Female Sexual Function Index.;Sleep quality scores in the Pittsburgh Sleep Quality Index. Timepoint: Measurement of sleep quality score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Pittsburgh Sleep Quality Index.;Depression scores in Beck depression Inventory. Timepoint: Measurement of depression score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Beck Depression Inventory.;Patient's treatment compliance. Timepoint: Measurement of treatment compliance score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Morisky Medication Adherence Scale.	—

Measure

Time frame

Sexual performance scores on Female Sexual Function Index. Timepoint: Measurement of women's sexual performance scores at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Female Sexual Function Index.;Sleep quality scores in the Pittsburgh Sleep Quality Index. Timepoint: Measurement of sleep quality score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Pittsburgh Sleep Quality Index.;Depression scores in Beck depression Inventory. Timepoint: Measurement of depression score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Beck Depression Inventory.;Patient's treatment compliance. Timepoint: Measurement of treatment compliance score at the beginning of the study, 10 weeks later, 22 weeks later. Method of measurement: Morisky Medication Adherence Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Abdi

Karaj University of Medical Sciences

fatemeh.abdi87@yahoo.com+98 26 3433 6007

Outcome results

None listed

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