aromatherapy: The Effect of Aroma Massage on Constipation

Sponsor
Mersin University (Other)
Overall Status
Completed
CT.gov ID
NCT05343910
Collaborator
(none)
48
1
2
3
16.2

Study Details

Study Description

Brief Summary

Advancing age arising changes in health status and systems adversely affect the quality of life of the elderly and the elderly face many complex health problems. Constipation is one of the common problems in the elderly. Therefore, The aim of this study is to examine effects of aromatherapy massage on constipation in the elderly.

Condition or Disease Intervention/Treatment Phase
  • Other: Aroma massage
N/A

Detailed Description

Old age is a physiological period of life in which various changes take place, meaning that the elderly must be given special consideration as a group with regard to health care. Advancing age arising changes in health status and systems adversely affect the quality of life of the elderly and the elderly face many complex health problems. Constipation is one of the common problems in the elderly. Insufficient liquid intake, insufficient or unsuitable diet, decreased mobility, the side effects of medication, underlying diseases, and rectal sensory-motor dysfunction are among the causes of constipation in the elderly. Constipation is a preventable and treatable problem, which if left untreated can cause physical and associated psychological problems such as back and waist pain, rectal pressure, loss of appetite, confusion, incontinence, nausea and vomiting, urinary dysfunction, fissure, rectal prolapse, hemorrhoids, intestinal obstruction, and syncope. Constipation can be managed using pharmacological methods, such as laxatives, enemas, suppositories, along with nonpharmacological procedures, such as changes in nutritional habits, fluid intake, education, activities to develop healthy intestinal habits, exercise, massage, aroma massage, biofeedback, stress management and acupuncture.

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Parallel AssignmentParallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Aroma Massage on Constipation in Elderly
Actual Study Start Date :
Dec 1, 2012
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Mar 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Aromatherapy massage group

Experimental: aromatherapy massage group The oil mixture used in this study (1:, 1:, 1: 1, 20cc rosemary, 20cc mint, 20cc ginger, 20cc black pepper), 80% of the mixture obtained from the total 4% (3.2cc) carrier oil (100% almond oil=96.8cc) and then combined with abdominal massage. Before implementing the procedure in the experimental group (n=25), information about what an abdominal and aroma massage is, how long it will take, and how it will be applied was provided to the participants. The older adult participants in the experimental group were applied aroma massage through gentle movements with slight pressure for 15 min a day, five days a week for three weeks.

Other: Aroma massage
The older adult participants in the experimental group were applied aroma massage through gentle movements with slight pressure for 15 min a day, five days a week for three weeks.

No Intervention: Control group

Individuals in the control group (n=24) did not receive any type of aroma massage application.

Outcome Measures

Primary Outcome Measures

  1. Stool consistency [change from before intervention, 3rd and 4th week of intervention]

    Small as marble, hard (1 point) Bulky, hard (2 points) Normal (3 points) Soft (4 points) Juicy (5 points) 7-day total value for stool consistency / 7-day total number of stools

  2. Amount of stool [change from before intervention, 3rd and 4th week of intervention]

    None (0 points) Less than the previous stool (1 point) Normal (2 points) a lot (3 points) 7-day total value for stool amount / 7-day total number of stools

  3. Straining during defecation [change from before intervention, 3rd and 4th week of intervention]

    Defecation without straining (1 point) Straining at the beginning of defecation (2 points) Straining at half defecation (3 points) Straining during the entire defecation (4 points) Obtained 7 days for straining during defecation total value / total number of defecations in 7 days

  4. 38 / 5.000 Çeviri sonuçları Full after defecation feeling of inability to ejaculate [change from before intervention, 3rd and 4th week of intervention]

    None after defecation (0 points) Present after defecation (1 point) 7 for the feeling of incomplete ejaculation after defecation. total value obtained per day / total number of defecations in 7 days

  5. Number of defecations [change from before intervention, 3rd and 4th week of intervention]

    How many defecations per day Total number of defecations in 7 days / 7

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 65 years and older

  • Communication and cooperation can be established

  • Conscious,, agreeing to participate in the research,

  • Decreasing bowel movements, not able to deactivate for 3 days or more

  • Living more than two of the complaints related to defecation, who have not undergone intestinal surgery before

  • Lesion or infection that disrupts skin integrity in the abdominal region, elderly without any problems such as heart disease and dementia

Exclusion Criteria:
  • had language problems

  • were below 65 years of age and

  • refused to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mersin University Mersin Turkey 33110

Sponsors and Collaborators

  • Mersin University

Investigators

  • Study Director: Mağfiret Kaşıkçı, Prof., Atatürk University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Didem Lafci, Principal Investigator, Mersin University
ClinicalTrials.gov Identifier:
NCT05343910
Other Study ID Numbers:
  • MersinUniversty
First Posted:
Apr 25, 2022
Last Update Posted:
Apr 25, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Didem Lafci, Principal Investigator, Mersin University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2022