Effect of Progressive Relaxation Exercises and TENS on Women Delivering Via Cesarean

Derya Öztürk Özen

Status: Completed

Conditions: Cesarean Section; Acute Pain

Treatments: Other: Progressive relaxation exercises (PRE); Device: Transcutaneous electrical neural stimulation (TENS); Other: Transcutaneous electrical neural stimulation (TENS) and Progressive relaxation exercises (PRE)

Study type: Interventional

Funder types: Other

Identifiers

NCT05511571

KA-17142

Details and patient eligibility

About

This study aimed to determine the effect of progressive relaxation exercises and transcutaneous electrical nerve stimulation administered to women delivering via cesarean section on acute pain, breastfeeding behavior, and comfort levels. Single-Blind, Randomized Controlled Study. This study was carried out in the obstetrics and gynecology clinic of a university hospital affiliated with the Ministry of Health in Turkey between August 20, 2018 and April 15, 2019. A total of 120 participants were randomly assigned to one of four groups, which included a transcutaneous electrical neural stimulation (TENS) group, a progressive relaxation exercises (PRE) group, a combined intervention (TENS+PRE) group, and a control group. Data were collected with a data collection form, the visual analogue scale (VAS), the LATCH breastfeeding diagnostic tool (LATCH), and the postpartum comfort scale (PCS). In the analysis of the data, numbers, percentages, and chi-square tests were used. Also, median values, Wilcoxon Signed-rank test, and Kruskal-Wallis H test were employed for continuous variables.

Enrollment: 120 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• women who were aged between 18 and 45,
• who were in the postoperative 8th hour,
• who had a transverse cesarean section,
• who, as well as their babies, did not develop any complications during pregnancy, delivery, and the postpartum period.

Exclusion criteria

• women who did not have an open wound on their body and/or allergic disease on their skin,
• who had cardiac arrhythmia or a pacemaker,
• who had a risk of epilepsy,
• who had epilepsy, eclampsia, kidney or liver disease,
• who had previously applied TENS and PRE methods,
• who were morbidly obese (with a BMI value of over 40),
• who used chronic opioids, antidepressants, and psychoactive drugs.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

120 participants in 4 patient groups

TENS group

Experimental group

Description:

Transcutaneous electrical neural stimulation (TENS)

Treatment:

Device: Transcutaneous electrical neural stimulation (TENS)

PRE group

Experimental group

Description:

Progressive relaxation exercises (PRE)

Treatment:

Other: Progressive relaxation exercises (PRE)

TENS+PRE group

Experimental group

Description:

Transcutaneous electrical neural stimulation (TENS) and Progressive relaxation exercises (PRE)

Treatment:

Other: Transcutaneous electrical neural stimulation (TENS) and Progressive relaxation exercises (PRE)

Control group

No Intervention group