Effects of Music Application and Gum Chewing on Pain, Anxiety, and Patient Satisfaction During Episiotomy Repair

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-49
SponsorSuleyman Demirel University

About this trial

Lacerations and episiotomies are serious procedures requiring surgical stitches. Therefore, pain occurs during episiotomy repair. Pain during episiotomy repair also causes anxiety, which in turn exacerbates pain. The goal of pain management is to alleviate pain without experiencing side effects. Midwives and nurses responsible for labor management play an active role in the use of nonpharmacological interventions to manage pain and anxiety during episiotomy repair.

No studies in the literature have been found that combine music and chewing gum during episiotomy repair. This study aims to determine the effects of music and chewing gum during episiotomy repair on pain, anxiety, and patient satisfaction.

This study will be to determine the effects of music and chewing gum during episiotomy repair on pain, anxiety, and patient satisfaction.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Study participation criteria

Women aged 18-49,

Primiparous,

Having a medio-lateral episiotomy,

Disqualifiers

Women who experienced deep lacerations (anal sphincter injuries, 3rd and 4th degree lacerations) during labor,

Those who underwent operative delivery (with vacuum or forceps),

Those with visual, hearing, or sensory impairments,

Those who were not diagnosed with a psychiatric disorder but had problems,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Music

    Behavioral

    No studies in the literature have investigated the use of music and chewing gum during episiotomy repair, nor the difference between them.

  • Gum Chewing

    Behavioral

    Women assigned to the gum group will chew plain gum between the beginning and end of the episiotomy repair (15-20 minutes). They will be asked to chew the same brand of easy-to-chew, sugar-free gum that does not contain sorbitol or xylitol. Sugar-free gum is preferred to avoid the risk of GI problems if swallowed with sorbitol-containing gum, and the risk of diarrhea if consumed in excess with xylitol. Given the risk of aspiration while chewing gum, the woman will be positioned in a semi-fowler position.

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Music groupExperimental treatment 1 intervention
Group B: Gum Chewing groupExperimental treatment 1 intervention
Group C: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Visual Analog Scale

The Visual Analog Scale (VAS) is used to assess pain intensity. The scale can be scored from 0 to 10 To be collected through a survey. The collected data were planned to be analyzed using SPSS with mean and standard deviation.

Time frame
The research period for a participant takes approximately 1 day
2

The PATIENT'S PERCEPTION SCALE

The PATIENT'S PERCEPTION SCALE scale was developed by Dopier et al. It was developed to measure patients' perceptions of nursing care and their satisfaction with it. The five-point Likert-type scale includes 15 statements regarding the quality of nursing care. Thus, The scale can be scored from 15 to 75. The scale can be scored from 20 to 80. The collected data were planned to be analyzed using SPSS with mean and standard deviation.

Time frame
The research period for a participant takes approximately 1 day
3

The State Anxiety Scale

The State Anxiety Scale (SAAS) was developed by Spielberger et al. The State Anxiety Scale has 20 items. It is used to measure anxiety symptoms. The items describing emotions and behaviors in the scale are scored on a 4-point Likert-type scale: "(1) Not at all," "(2) A little," "(3) A lot," and "(4) Completely." The scale can be scored from 20 to 80. The scale can be scored from 20 to 80 The collected data were planned to be analyzed using SPSS with mean and standard deviation.

Time frame
The research period for a participant takes approximately 1 day

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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