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Effect of Abdominal Massage on Excretory Activity and Pulmonary Function Tests in Patients After Surgery

M

Mersin University

Status

Completed

Conditions

Intraabdominal Pressure

Treatments

Other: Abdominal massage

Study type

Interventional

Funder types

Other

Identifiers

NCT05127577
MersinUCKANAT-01

Details and patient eligibility

About

This study is aimed to determine the effect of abdominal massage on excretory activity and pulmonary function tests (PFT) in patients undergoing PKP.

Full description

Methods: The research will be carried out with 78 patients who underwent partial hip replacement. Patients were assigned to study (abdominal massage) and control groups by randomization. Abdominal massage will be applied to the patients at least 30 minutes after the morning and evening meals (08:30 in the morning, 20:30 in the evening) for 15 minutes, similar to the literature. Patients' data will be collected 15 minutes before and after the application of abdominal massage. Within the scope of the patient's data, information on pulmonary function test values, intra-abdominal pressure value and excretory activities will be collected. Abdominal massage will start in the evening of the day the patient is transferred to the clinic (20:30), and will be terminated when the patient defecates. No treatment will be applied to the patients in the control group. The data recorded before and after the abdominal massage in the study group will be recorded in the Excretory Activity Form and the Pulmonary Function Test Form as a result of the measurements made at the same time in the control group.

Enrollment

78 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having a urinary catheter for at least one day after surgery,
  • Discharged at least 48 hours after surgery,
  • Do not have any condition for which abdominal massage is contraindicated (inflammatory bowel disease, presence of abdominal tumor, surgical intervention or radiotherapy to the abdominal region, presence or suspicion of ileus, and pregnancy),
  • No diagnosis of chronic constipation made by a physician,
  • Who has not developed any respiratory tract complications (atelectasis, pneumonia, etc.) due to surgical intervention,
  • No chronic respiratory disease (chronic obstructive pulmonary disease, pulmonary hypertension, sleep apnea syndrome, asthma, chronic bronchitis, cystic fibrosis, occupational lung diseases, etc.),
  • Patients who do not have problems in transition to oral feeding and who can be fed orally will be included in the study.

Exclusion criteria

  • Urinary catheter removed within the first day after surgery,
  • Discharged before 48 hours after surgery,
  • Any condition in which abdominal massage is contraindicated (inflammatory bowel disease, presence of abdominal tumor, surgical intervention or radiotherapy to the abdominal region, presence or suspicion of ileus, and pregnancy),
  • Having a diagnosis of constipation made by a physician,
  • Having any respiratory complications (atelectasis, pneumonia, etc.) developed due to surgical intervention,
  • Having chronic respiratory disease (chronic obstructive pulmonary disease, pulmonary hypertension, sleep apnea syndrome, asthma, chronic bronchitis, cystic fibrosis, occupational lung diseases, etc.),
  • Patients who have problems in the transition to oral feeding and cannot be fed orally will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

78 participants in 2 patient groups

Abdominal massage group
Experimental group
Description:
Abdominal massage will be applied to the experimental group 2 times a day, morning and evening, until defecation, starting in the evening of the first day after the surgical intervention.
Treatment:
Other: Abdominal massage
Control group
No Intervention group
Description:
The control group will be received routine treatment and care in the unit.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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