Effect of Therapeutic Touch at Different Times on Infantile Colic According to Watson's Theory

Sponsor
Karamanoğlu Mehmetbey University (Other)
Overall Status
Completed
CT.gov ID
NCT05244291
Collaborator
(none)
96
1
3
4.3
22.5

Study Details

Study Description

Brief Summary

Aim: The purpose of the study is to determine the effect of therapeutic touch applied to infants with infantile colic at different times on infant colic scale score, crying and sleep duration, according to Watson's theory of human care. Thus, it is aimed to contribute to the development of an effective care approach in eliminating or reducing the symptoms in infants with infantile colic.

Method: The study will be conducted as a single-blind, randomized controlled trial. The population of the study will be infants who come to the Pediatrics Outpatient Clinic and are diagnosed as infantile colic according to the evaluation of the pediatrician and have no other health problems. The infants will be divided into three groups as intervention (The first group; the group in which therapeutic touch was applied for one week and the second group; the group in which the therapeutic touch was applied for two weeks) and control groups according to stratified block randomization in the computer environment. After the randomization, therapeutic touch will be applied to the intervention group. No method will be applied to the control group.

Condition or Disease Intervention/Treatment Phase
  • Other: Therapeutic Touch
N/A

Detailed Description

The research will be carried out with three groups as intervention (The first group; the group in which therapeutic touch was applied for one week and the second group; the group in which the therapeutic touch was applied for two weeks) and control groups. Sample size of the study has been determined by the power analysis, in line with the results obtained from the studies which have been conducted using a similar research method. According to the analysis results, it has been calculated as 32 for each group and 96 in total. Mothers of the infants meeting the study inclusion criteria will be informed both in written and verbally. Written consent will be obtained. The infants will be divided into three groups according to block randomization in the computer environment. The randomization, therapeutic touch will be applied to the intervention group (The first group; the group in which therapeutic touch was applied for one week and the second group; the group in which the therapeutic touch was applied for two weeks). No method will be applied to the control group by the researcher. In obtaining research data, 4 tools will be used: "Mother-infant Information Form", "Infantile Colic Scale", Crying Time Registration Form and Sleep Time Registration Form.

Study Design

Study Type:
Interventional
Actual Enrollment :
96 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study will be conducted as a single-blind, randomized controlled trial.The study will be conducted as a single-blind, randomized controlled trial.
Masking:
Single (Participant)
Masking Description:
Single blind will be done in the study. Only parents will be blinded. Two weeks follow up will be done in both groups. Since the researcher should implement the intervention, evaluate and manage the process, it will not be blinded.
Primary Purpose:
Supportive Care
Official Title:
The Effect of Therapeutic Touch at Different Times on Colic Symptoms in Infants With Infantile Colic According to Watson's Theory of Human Care: A Randomized Controlled Study
Actual Study Start Date :
Mar 25, 2022
Actual Primary Completion Date :
May 28, 2022
Actual Study Completion Date :
Aug 2, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group 1

Therapeutic Touch will be applied to infants for 3 consecutive days, once a day, 10 minutes at any time during the day. There will be a four-day break. The Therapeutic Touch will be done a total of 3 times in 1 weeks.

Other: Therapeutic Touch
Therapeutic Touch will be applied to infants for 3 consecutive days, once a day, 10 minutes at any time during the day. There will be a four-day break. The Therapeutic Touch will be done a total of 3 times a week or 6 times in 2 weeks.

Experimental: Intervention Group 2

Therapeutic Touch will be applied to infants for 3 consecutive days, once a day, 10 minutes at any time during the day. There will be a four-day break. The Therapeutic Touch will be done a total of 6 times in 2 weeks.

Other: Therapeutic Touch
Therapeutic Touch will be applied to infants for 3 consecutive days, once a day, 10 minutes at any time during the day. There will be a four-day break. The Therapeutic Touch will be done a total of 3 times a week or 6 times in 2 weeks.

No Intervention: Control Group

The therapeutic touch will not be applied to the control group infants. However, the routine follow-up and behavior of the weekly baby will be evaluated to ensure that parents are blind.

Outcome Measures

Primary Outcome Measures

  1. Crying Time [In eight weeks.]

    Infants' weekly crying times will be recorded (Every day of the week). Weekly crying time will be taken.

  2. Sleeping Time [In eight weeks.]

    Infants' weekly sleeping times will be recorded (Every day of the week). Weekly sleeping time will be taken.

Secondary Outcome Measures

  1. Infantile Colic Scale [In eight weeks.]

    Ellet et al. (2002) developed a Likert-type scale to determine the factors causing colic and to diagnose colic. Cetinkaya and Başbakkal (2007) tested the validity and reliability of the scale for the Turkish population. The scale consists of 5 sub-dimensions and 19 items.The low total score average from the scale indicates that the colic decreases, and the high average score indicates that the colic increases. Infantile colic scale will be applied to all babies in the study when they complete these weeks.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Weeks to 8 Weeks
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Family volunteering to participate in the research

  • The infant was born at term

  • The infant is between 4 weeks and 8 weeks

  • The birth weight is between 2500-4500 g

  • The infant has been diagnosed with infantile colic by a physician

  • Mothers' ability to read, write and speak Turkish

  • New diagnosis of infantile colic

Exclusion Criteria:
  • The baby has any chronic disease

  • The baby has a congenital anomaly

  • The mother has a diagnosed mental and mental problem

  • Mother's smoking

  • The diagnosis of infants with lactose intolerance by the physician

Contacts and Locations

Locations

Site City State Country Postal Code
1 Karaman Education and Research Hospital Karaman Turkey

Sponsors and Collaborators

  • Karamanoğlu Mehmetbey University

Investigators

  • Principal Investigator: Selda Ateş Beşirik, Res. Assist. Dr., Karamanoğlu Mehmetbey University
  • Study Director: Emine Geçkil, Professor, Necmettin Erbakan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Selda Ateş Beşirik, Karamanoğlu Mehmetbey University, Faculty of Health Science, Pediatric Nursing Department, Karamanoğlu Mehmetbey University
ClinicalTrials.gov Identifier:
NCT05244291
Other Study ID Numbers:
  • 05-2021/27
First Posted:
Feb 17, 2022
Last Update Posted:
Aug 3, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Selda Ateş Beşirik, Karamanoğlu Mehmetbey University, Faculty of Health Science, Pediatric Nursing Department, Karamanoğlu Mehmetbey University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 3, 2022