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NCT Number: NCT07338747

Educational Video, Anxiety, and Mode of Delivery After Previous Cesarean

This interventional study evaluates whether video-based patient education regarding Trial of Labor After Cesarean (TOLAC) reduces maternal anxiety compared with standard verbal counseling. Pregnant women eligible for TOLAC will be randomized to receive either a structured educational video or routine verbal counseling. Maternal anxiety levels will be assessed using the State-Trait Anxiety Inventory (STAI).

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

Trial of labor after cesarean (TOLAC) is a complex clinical decision that may be associated with significant maternal anxiety. Adequate counseling is essential to support informed decision-making; however, the optimal method for delivering information remains unclear.

This randomized interventional study aims to assess whether video-based patient education can reduce anxiety levels compared with standard verbal counseling. Eligible pregnant women planning delivery after a previous cesarean section will be randomly assigned to one of two study arms: video-based educational counseling or standard verbal counseling.

Anxiety will be measured using the validated State-Trait Anxiety Inventory (STAI) questionnaire after counseling. The results of this study may inform future strategies for patient counseling and shared decision-making in women considering TOLAC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women with a singleton pregnancy.
  • History of one previous cesarean delivery with a low transverse uterine incision.
  • Eligible for a trial of labor after cesarean (TOLAC) according to clinical assessment and Israeli national clinical guidelines.
  • Age 18 years or older.
  • Hebrew-speaking.
  • Ability and willingness to provide written informed consent.

Exclusion criteria

  • Medical or obstetric conditions contraindicating vaginal delivery, including but not limited to placenta previa or marginal placenta previa.
  • History of uterine surgery other than one prior low transverse cesarean section that precludes vaginal delivery.
  • History of two or more prior cesarean deliveries.
  • Non-vertex fetal presentation or any presentation unsuitable for a trial of labor.
  • Multiple gestation.
  • Diagnosed severe anxiety disorder or other significant psychiatric disorder that may interfere with participation in the study or completion of questionnaires.

Treatment and study plan

Video-Based Educational Intervention

Behavioral

A structured educational video providing information on benefits, risks, and expectations of trial of labor after cesarean.

Standard Verbal Counseling

Other

Routine verbal counseling provided by the treating clinician regarding trial of labor after cesarean.

Primary outcomes

  1. Maternal Anxiety Level

    Time frame: Immediately after completion of counseling.

    Assessment of maternal anxiety using the State-Trait Anxiety Inventory (STAI) questionnaire.

Secondary outcomes

  1. Patient Knowledge Regarding Trial of Labor After Cesarean

    Time frame: Immediately after completion of counseling.

    Assessment of patient knowledge regarding trial of labor after cesarean, based on a structured questionnaire developed for the study.

  2. Rate of Successful Trial of Labor After Cesarean (TOLAC)

    Time frame: From delivery.

    Proportion of participants who achieved a successful vaginal birth following a trial of labor after cesarean.

  3. Patient Satisfaction With Counseling Method

    Time frame: Immediately after completion of counseling.

    Patient-reported satisfaction with the counseling method received (video-based education or standard verbal counseling), assessed using a Likert-scale questionnaire.

  4. Maternal Preference for Trial of Labor After Cesarean Versus Elective Repeat Cesarean Delivery

    Time frame: Immediately after completion of counseling.

    Participant-reported preference for mode of delivery (trial of labor after cesarean versus elective repeat cesarean delivery) following counseling.

Study contacts

Contact information is provided by the study sponsor or research team.

Shir Lev, MD

CONTACT

[email protected]

+972504598339

Sponsors and collaborators

Lead sponsor

Wolfson Medical Center

Other Gov

Registry information

Official study title

Does an Educational Video Increase Trial of Labor After Cesarean and Reduce Anxiety Among Women With a Prior Cesarean? A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Jan 14, 2026
Registry last updated
Jan 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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