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Investigating the effectiveness of mindfulness based cognitive therapy (MBCT) on stress and life expectancy in infertile women undergoing acupuncture treatment

Investigating the effectiveness of mindfulness based cognitive therapy (MBCT) on stress and life expectancy in infertile women undergoing acupuncture treatment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240623062228N1
Enrollment
40
Registered
2024-07-25
Start date
2024-07-27
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Female infertility. Female infertility

Interventions

Intervention 1: Intervention group: 8 intervention sessions will be implemented based on the treatment plan of Williams et al (1952). This intervention consists of eight one-and-a-half-hour weekly gro

Sponsors

Islamic Azad University, Semnan branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Infertile women with an age range of 20 to 40 years. Diagnosis of infertility by a specialist doctor. Receiving acupuncture treatment for infertility. Ability and willingness to participate in 8 cognitive therapy intervention sessions based on mindfulness. Not having diagnosed severe mental disorders (such as schizophrenia, bipolar disorder). Ability to read and write in order to fill out questionnaires and do homework. Written consent to participate in the study and follow the research instructions.

Exclusion criteria

Exclusion criteria: Existence of severe physical problems that prevent regular attendance at meetings. Currently taking psychotropic or antidepressant medications. Pregnancy or planning to become pregnant during the study period. History of participating in similar cognitive therapy programs based on mindfulness in the past year. Unwillingness to continue acupuncture treatment during the study period. Inability to do mindfulness exercises due to cognitive or physical problems. Any other condition that the researcher considers to be an obstacle to effective participation in the study.

Design outcomes

Primary

MeasureTime frame
Stress score. Timepoint: Before the start of the intervention (pre-test), after completing 8 sessions of the intervention (post-test), one month after the end of the intervention (follow-up). Method of measurement: Newton et al. stress test (1999).;Life expectancy score. Timepoint: Before the start of the intervention (pre-test), after completing 8 sessions of the intervention (post-test), one month after the end of the intervention (follow-up). Method of measurement: Miller's Life Expectancy Test (1988).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArezou Nouri shafie

Islamic Azad University, Semnan branch

arezounoori66@gmail.com+98 21 3611 1111

Outcome results

None listed

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