Investigate the impact of counseling on acceptance and commitment therapy to the fear, attitude and intention of choosing the type of delivery

Investigate the impact of counseling with an approach based on acceptance and commitment therapy to the fear, attitude and intention of choosing the type of delivery in primigravid women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180901040916N1

Enrollment

Registered

2019-05-13

Start date

2018-10-02

Completion date

Unknown

Last updated

2019-05-21

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

Conditions

Fear of delivery, Attitude of delivery , Intent to choose the type of delivery. Maternal distress during labour and delivery

Interventions

Intervention 1: Intervention group: Receiving 4 consultation sessions with an approach base on acceptance and commitment therapy in group ,any week ,a meeting with a duration of 90 to 120 minute up to

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1- Residence in Mashhad 2- Access to Telephone 3- Having at least elementary education 4- Do not have a mother's hearing and speech problems that can not communicate with a researcher 5- Age between 18 and 35 6- Gestational age between 28 weeks to 32 weeks 7- Single and low-risk pregnancy 8- Primigravid 9- Willingness to cooperate 10- The sample has no history of infertility 11- The sample does not have a medical cause for cesarean section (such as a transverse or transverse placement, an uterine surgeon, etc.).

Exclusion criteria

Exclusion criteria: 1- Do not be staffed by a hospital 2- She has not had severe mental problems in the last 6 months 3- In the Vijma's fear questionnaire, she scored less than 85 points

Design outcomes

Primary

Measure	Time frame
Fear of delivery. Timepoint: At the beginning of the study, then immediately and one week after the intervention. Method of measurement: Vijma's fear of delivery Questionnaire; Version A.;Attitude towards delivery. Timepoint: At the beginning of the study and then immediately and one week after the intervention. Method of measurement: Attitude to the type of delivery questionnaire.;Intent to choose the type of delivery. Timepoint: At the beginning of the study and then immediately and one week after the intervention. Method of measurement: Intent selection choose the type of delivery checklist.;Social support. Timepoint: At the beginning of the study. Method of measurement: Modified Cassidy Social Support Assessment Questionnaire.;Decision Conflict. Timepoint: At the beginning of the study. Method of measurement: Decision Conflict Questionnaire.;Self-efficacy of delivery. Timepoint: At the beginning of the study. Method of measurement: Maternal self-efficacy questionnaire.	—

Measure

Time frame

Fear of delivery. Timepoint: At the beginning of the study, then immediately and one week after the intervention. Method of measurement: Vijma's fear of delivery Questionnaire; Version A.;Attitude towards delivery. Timepoint: At the beginning of the study and then immediately and one week after the intervention. Method of measurement: Attitude to the type of delivery questionnaire.;Intent to choose the type of delivery. Timepoint: At the beginning of the study and then immediately and one week after the intervention. Method of measurement: Intent selection choose the type of delivery checklist.;Social support. Timepoint: At the beginning of the study. Method of measurement: Modified Cassidy Social Support Assessment Questionnaire.;Decision Conflict. Timepoint: At the beginning of the study. Method of measurement: Decision Conflict Questionnaire.;Self-efficacy of delivery. Timepoint: At the beginning of the study. Method of measurement: Maternal self-efficacy questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahboobeh firoozi

Mashhad University of Medical Sciences

firoozim@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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