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Aromatherapy Massage Applied on Constipation

A

Ayşe Aydınlı

Status

Completed

Conditions

Constipation

Treatments

Other: Aromatherapy Massage

Study type

Interventional

Funder types

Other

Identifiers

NCT04513093
SuleymanDU Aaydinli

Details and patient eligibility

About

Aim: This study was conducted as a randomized controlled experimental study to examine the effect of abdominal massage with ginger and lavender oil on constipation in elderly individuals.

Design: The study was completed with 40 elderly individuals in Kayseri nursing home, including 20 in intervention and 20 in control group who met the criteria for inclusion in the study. In the study, written informed volunteer consent was obtained from the individuals with the approval of the ethics committee and the permission of the institution.

The elderly individuals in the intervention group underwent aromatherapy massage with ginger and lavender oils for a period of five days and 15 minutes on weekdays for four weeks according to the abdominal massage application protocol. No application was made to individuals in the control group.

Full description

Aim: This study was conducted as a randomized controlled experimental study to examine the effect of abdominal massage with ginger and lavender oil on constipation in elderly individuals.

Design: The study was completed with 40 elderly individuals in Kayseri nursing home, including 20 in intervention and 20 in control group who met the criteria for inclusion in the study. In the study, written informed volunteer consent was obtained from the individuals with the approval of the ethics committee and the permission of the institution. The data were collected by the researcher using the Questionnaire Form, Bristol Stool Scale, Rome IV Criteria, Constipation Severity Scale and Mini Mental Test.

The elderly individuals in the intervention group underwent aromatherapy massage with ginger and lavender oils for a period of five days and 15 minutes on weekdays for four weeks according to the abdominal massage application protocol. No application was made to individuals in the control group. The "Bristol Stool Scale" and "Constipation Severity Scale" were re-applied to the individuals in the intervention and control group before, during the second week of practice and at the end of practice (fourth week).

Enrollment

40 patients

Sex

All

Ages

65 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elderly individuals with constipation determined by the institution doctor,
  • Individuals diagnosed with constipation according to the Roma-criteria,
  • Individuals, who achieved a score of 24 and higher on the standardized mini mental test (SMMT),
  • Individuals, who do not have lesions disrupting skin integrity in the abdominal region,
  • And elderly individuals, who agreed to participate in the study were included.

Exclusion criteria

  • Individuals diagnosed with irritable bowel syndrome (IBS),
  • Individuals who have undergone bowel surgery before,
  • Individuals diagnosed with colon cancer,
  • Individuals with percutaneous endoscopic gastrostomy,
  • Individuals with umbilical hernia
  • And individuals allergic to lavender and ginger oil.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

İntervention Group
Experimental group
Description:
The elderly individuals in the intervention group underwent aromatherapy massage with ginger and lavender oils for a period of five days and 15 minutes on weekdays for four weeks according to the abdominal massage application protocol. The "Bristol Stool Scale" and "Constipation Severity Scale" were re-applied to the individuals in the intervention before, during the second week of practice and at the end of practice (fourth week).
Treatment:
Other: Aromatherapy Massage
Control Group
No Intervention group
Description:
No application was applied to the individuals in the control group. "Bristol Stool Scale" and "Constipation Severity Scale" were applied to the individuals in the control group at the same time as (at the beginning, second week and fourth week) the intervention group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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