The Effect of Guided Imagery on Bonding and Breastfeeding After Cesarean

Sponsor
Menekşe Nazlı AKER (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05344846
Collaborator
(none)
64
2
7

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the effect of guided imagery after cesarean section on mother-infant bonding and breastfeeding.

The study will be carried out in two different groups. The practice will start with meeting the women 6-10 hours after cesarean section. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Intervention Group; The individuals in this group will be provided with guided imagery application. Guided imagery will be applied to the participants in the hospital environment 6-10 hours after the cesarean section. Afterwards, guided imagery application will be requested every day for two weeks.

Control Group; The participants in the control group will perform routine care of the clinic.

Condition or Disease Intervention/Treatment Phase
  • Other: Guided imagery
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Guided Imagery on Bonding and Breastfeeding After Cesarean; A Randomized Controlled Study
Anticipated Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Guided imagery Group

Guided imagery after cesarean

Other: Guided imagery
The individuals in this group will be provided with guided imagery application. Guided imagery will be applied to the participants in the hospital environment 6-10 hours after the cesarean section. Afterwards, guided imagery application will be requested every day for two weeks.

No Intervention: Standard care

The participants in the control group will perform routine care of the clinic.

Outcome Measures

Primary Outcome Measures

  1. Change in how to feed baby [Baseline, 7th day, 14th day]

    Nutrient content that she feeds her baby (Breastmilk, formula etc)

  2. Change in The Mother-to-Infant Bonding Scale [Baseline, 7th day, 14th day]

    The scale consists of eight adjectives (loving, resentful, neutral or felt nothing, joyful, dislike, protective, disappointed and aggressive), each followed by a four-point Likert scale ranging from "Very much" (0) to "Not at all" (5). When the adjective reflects a negative emotional response, the scoring is reversed. Thus, possible scores on the scale range between 0 and 24, with high scores indicating a problematic mother-to-infant bond (Taylor et al. 2005).

  3. Change in Breastfeeding Self-Efficacy Scale [Baseline, 7th day, 14th day]

    The 14-item scale was developed by Dennis (2003). The scale is a 5-point Likert-type scale (1= 'I am not sure at all' and 5 = 'I am always sure'). The scale's minimum score is 14 and the maximum score is 70. An elevated score shows an increase in breastfeeding self-efficacy.

Secondary Outcome Measures

  1. Change in Perception of Insufficient Milk Questionnaire [Baseline, 7th day, 14th day]

    This scale, developed by McCarter-Spaulding for determining the perception of insufficient breast milk, is a six-question form. The scale's minimum score is 0 and the maximum score is 50. A high total score indicates that milk sufficiency perception is also high.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Nullipar

  • Single birth

  • Baby being with mother

  • Gestational age 37-42 weeks

  • Birth weight between 2500-4000 g

  • APGAR score of 7 or higher in the 1st and 5th minutes

  • The mother does not have a health problem that prevents breastfeeding

  • Absence of conditions that prevent sucking, such as frenulum or palate problems

Exclusion Criteria:
  • Participant's non-compliance with the research plan

  • Interruption of breastfeeding for reasons such as health problems of the mother or baby

  • Participants receive professional support for breastfeeding during the study process

  • Hearing loss and deafness

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Menekşe Nazlı AKER

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Menekşe Nazlı AKER, Assist. Prof., Ankara University
ClinicalTrials.gov Identifier:
NCT05344846
Other Study ID Numbers:
  • 0555
First Posted:
Apr 25, 2022
Last Update Posted:
May 2, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 2, 2022