The Effect Of White Noise And Therapeutic Touch On Pain And Physiological Parameters In Premature Infants

NCT ID: NCT05395208

Last Updated: 2022-05-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 81 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-01
• Study Completion Date: 2022-01-12

Brief Summary

Newborns hospitalized with some respiratory problems in the clinic are taken to noninvasive mechanical ventilation support and vascular access is required for some treatments to be applied to these newborns. The presence of nasal cannulas used for noninvasive mechanical ventilation support in newborns causes restlessness, agitation and stress in infants. The uneasiness and stress experienced by babies during vascular access also affects effective vascular access, causing other doses to be delayed or skipped due to treatment doses that are not completed on time. In addition, the pain experienced by babies indirectly affects nurses. It has been reported in many studies that it is effective in reducing the pain experienced by newborns with non-pharmacological methods. Simultaneous white noise will be played and therapeutic touch applied to help touch methods and white noise listening help reduce or control newborns' pain. Many studies have shown that touching to and listening white noise is effective in reducing pain. This study was planned as a randomized controlled experimental study to determine the effect of white noise-accompanied therapeutic touch application on pain level and physiological parameters and noninvasive mechanical ventilation support during peripheral intravenous catheterization in premature infants hospitalized for treatment.

Hypothesis 0: The application of therapeutic touch with white noise during peripheral intravenous catheter intervention in premature infants has no effect on the level of pain.

Hypothesis 1: White noise-accompanied therapeutic touch application reduces pain level during peripheral intravenous catheter intervention in premature infants.

Hypothesis 2: The therapeutic touch application accompanied by white noise during peripheral intravenous catheter intervention in premature infants positively affects physiological parameters.

Detailed Description

Purpose of the research The study was planned as a randomized controlled experimental study to determine the effect of white noise and therapeutic touch on pain level and physiological parameters and noninvasive mechanical ventilation support during peripheral intravenous catheter intervention in hospitalized premature infants.

As a data collection tool; "Baby Follow-up Form" was used in which some descriptive features of the baby and NIPS and physiological parameter measurements were evaluated.

Application:

The data of the study were collected using simple random sampling method. The newborns to be included in the study were divided into two groups as the intervention group and the control group. The data were determined according to the odd and even numbered days of the calendar between the research dates, and the babies born on the odd numbered days of the calendar were included in the white noise therapeutic touch group (intervention group), and the babies born on the even numbered days of the calendar were included in the control group. The environmental conditions in the two groups were regulated in the same way. The application was carried out with a research nurse performing therapeutic touch, an observer nurse and a practitioner nurse.

Intervention Group (n=40) :

• Camera recording was started 5 minutes before intravenous catheter intervention, vital signs and pain were evaluated.
• Therapeutic touch application with white noise was started.
• Vital signs and pain were evaluated during intravenous catheterization.
• Vital signs and pain were evaluated when the intravenous catheter intervention was terminated and 5 minutes later, and the camera recording was stopped.

Control Group (n=41):

• Camera recording was started 5 minutes before the intravenous catheter intervention, vital signs and pain were evaluated.
• No application was made other than intravascular catheter intervention.
• Vital signs and pain were evaluated during intravenous catheterization.
• Vital signs and pain were evaluated when the intravenous catheter intervention was terminated and 5 minutes later, and the camera recording was stopped.

Universe and Research Example Newborns treated at Zeynep Kamil Gynecology and Pediatrics Training and Research Hospital Neonatal Intensive Care Service between June 2021 and January 2022 constitute the population of the research. The sample of the study consisted of 85 newborns meeting the sampling criteria of the study in the Neonatal Intensive Care Service of Zeynep Kamil Gynecology and Pediatrics Training and Research Hospital.

Sampling selection criteria of the infant;

• 32-36. to be born in gestational weeks,
• The need for noninvasive mechanical ventilation,
• Absence of congenital anomalies,
• Appropriate cognitive level and motor development of the newborn,
• Does not prevent the opening of the vascular access,
• Not using narcotic, sedative opioid and anticonvulsant drugs,
• No pharmacological intervention for the baby's pain during the procedure,
• Parents sign the informed consent form. Dependent Variables: The newborn's heart rate, respiratory rate, oxygen saturation, body temperature, blood pressure, pain score are the dependent variables.

Independent Variables: The sex of the newborn, gestational age, mode of delivery, weight, height, head circumference, type of feeding, type of noninvasive mechanical ventilation support constitute the independent variables.

Sample size was determined by power analysis. In the study, the power of the sample was calculated with the G*Power 3.1 program. The amount of type I error was 0.05 and the power of the test =0.80 (α=0.05, 1-β=0.80, effect size:0.6), while the minimum sample size (36 newborns in each group) was 72. newborns Considering the losses that may arise from the sample for any reason during the study period, it is planned to take 10% more of the power analysis result. In the study, 40 newborns were included in the intervention group (therapeutic touch with white noise) and 41 newborns in the control group.

Data Collection Written permission from the ethics committee of Zeynep Kamil Gynecology and Pediatrics Training and Research Hospital (Annex-3) and research permission from the Istanbul Governorship Provincial Health Directorate (Annex-4) for the collection of pre-research data. After explanations were given to the families of the newborns who agreed to participate in the study, and to the families of the newborns who met the sample selection criteria for the purpose of the study, verbal and written informed consent was obtained from the families of the newborns who agreed to participate in the study (Annex-1). During the research, personal information will be kept confidential and care will be taken for their privacy. The data of the study were collected between June 2020 and January 2021. The application time of each data and filling the data collection forms took an average of 20-25 minutes.

Evaluation of Data The data of the study were analyzed with appropriate statistical methods using the SPSS (Statistical Package for the Social Science) 22.0 package program. In the evaluation of the data, percentage, number, mean and standard deviation were used as descriptive statistical methods, and frequency and percentage distributions of the data were given. The relationship between the variables measured at the categorical level was evaluated with the Pearson chi-square test. Whether the research variables showed normal distribution or not was examined by paired test and independent group t test. The significance level was 0.05; It was stated that there was a significant difference in cases with p<0.05, and there was no significant difference in cases with p>0.05.

Conditions

Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Therapeutic touch group accompanied by white noise

• Camera recording was started 5 minutes before intravenous catheter intervention, vital signs and pain were evaluated.
• Therapeutic touch application with white noise was started.
• Vital signs and pain were evaluated during intravenous catheterization.
• Vital signs and pain were evaluated when the intravenous catheter intervention was terminated and 5 minutes later, and the camera recording was stopped.

Group Type: EXPERIMENTAL

Therapeutic touch group accompanied by white noise

Intervention Type: BEHAVIORAL

During the intravenous catheter intervention, approximately 15-20 minutes of white noise was applied with therapeutic touch.

Control group

• Camera recording was started 5 minutes before the intravenous catheter intervention, vital signs and pain were evaluated.
• No application was made other than intravascular catheter intervention.
• Vital signs and pain were evaluated during intravenous catheterization.
• Vital signs and pain were evaluated when the intravenous catheter intervention was terminated and 5 minutes later, and the camera recording was stopped.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Therapeutic touch group accompanied by white noise

During the intravenous catheter intervention, approximately 15-20 minutes of white noise was applied with therapeutic touch.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• To be in noninvasive mechanical ventilation support,
• Newborns between 32-36 weeks,
• Not having a life-threatening disease,
• No congenital anomalies,
• Appropriate cognitive level and motor development of the newborn,
• The newborn does not have a physical problem,
• Parents' willingness to participate in the research,

Exclusion Criteria

• Presence of IV catheter,
• Having a condition that prevents vascular access,
• Those who have circulation problems in the body,
• Using narcotic, sedative opioid and anticonvulsant drugs
• Pharmacological intervention application for the baby's pain during the procedure

• Minimum Eligible Age: 32 Weeks
• Maximum Eligible Age: 36 Weeks
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Okan University

OTHER

Sponsor Role: lead

Responsible Party

Zeynep Uysal

NURSE

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Gülzade Uysal, Assoc. Dr.

Role: STUDY_DIRECTOR

Okan Üniversitesi

Locations

Home/Work

Istanbul, Üsküdar, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

2021/99

Identifier Type: -

Identifier Source: org_study_id