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Comparison of the effect of cognitive counseling versus routine care on adaptation of women with unplanned pregnancy

Comparison of the effect of cognitive counseling versus routine care on adaptation of women with unplanned pregnancy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017042228352N5
Enrollment
54
Registered
2017-10-01
Start date
2017-08-12
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Unplanned pregnancy. Problems related to unwanted pregnancy

Interventions

Intervention 1: The intervention group will be 27 people that nine people in each group will participate in counseling sessions.Consultations with the intervention group will be done by the researcher
The intervention group will be 27 people that nine people in each group will participate in counseling sessions.Consultations with the intervention group will be done by the researcher in 8 sessions i
Control group: in this group no counseling will be received and only the routine pregnancy care will be done.At the end of the study, educational pamphlets and packages, which gave to the intervention

Sponsors

Vice chancellor for research, Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Should have unplanned pregnancy; To be interested to participate in the study; Lacking the history of obstetric complications, psychological disease and medicine use; Gestational age less than 14 weeks; Lack of known psychological disease; Be married (and live with her husbands); Pregnant woman has an alive mother; Lack of narcotic substances abuse in women or her husbands; At least have secondary school education. Exclusion criteria: The unwillingness to continue the cooperation in the study; Non-participation in two or more than two sessions of counseling; Incidence of any pregnancy complications such as abortion and fetal death;The occurrence of any stressor event or accident during the study; The incidence of any clinical conditions in patients, which cause to impossibility of the intervention; Incompleteness of the questionnaires so that more than 20% of questions are unanswered.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Adaptation of unplanned pregnancy. Timepoint: At baseline, immediately after the intervention and one month after the Last counseling session. Method of measurement: Prenatal self-evaluation questioner.

Secondary

MeasureTime frame
Quality of life. Timepoint: At baseline, immediately after the intervention and one month after the Last counseling session. Method of measurement: World Health Organization quality of lifes questioner-26.;Maternal-fetal attachment. Timepoint: At baseline, immediately after the intervention and one month after the Last counseling session. Method of measurement: Cranley’s maternal-fetal attachment scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Arasteh

Zanjan University of Medical Science

Azadearaste@yahoo.com+98 56 3272 4212

Outcome results

None listed

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