The Effect of Aromatherapy Massage Applied to Hemodialysis Patients With Muscle Cramp

NCT ID: NCT04874857

Last Updated: 2023-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-25

Study Completion Date

2022-12-28

Brief Summary

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This study is a randomized controlled and single-blind study consisting of qualitative and quantitative stages to evaluate the effect of aromatherapy massage on cramp frequency, cramp pain severity and quality of life in crampy hemodialysis (HD) patients.

Detailed Description

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Data-collecting interviewers are blind to which patients are in which group. The days and sessions of the groups were randomly determined after patients meeting the research criteria of the intervention, placebo control, and control groups were ranked.

The population of the study consists of 566 patients treated in institutions that allow the research to be conducted.

145 patients participated in the study and the study was terminated with 94 patients. In the study, aromatherapy massage was applied to the intervention group, baby oil massage was applied to the placebo control group, while no application was made to the control group other than routine care. Aromatherapy massage to the intervention group; It was applied with a mixture of 7% lavender, rosemary and marjoram essential oils.

Dependent Variables: Cramp frequency, mean cramp pain severity, and quality of life scale total score.

Independent Variables: age, gender, body mass index, marital status, educational status, income level, sociodemographic characteristics such as smoking and alcohol use, characteristics related to the diagnosis-treatment process, concomitant diseases and laboratory parameters.

Research data; Intervention and Placebo Group Situation Evaluation Chart, Personal Information Form, Personal Interview Form, Visual Analogue Scale, Quality of Life Index Dialysis Version-III and Control, Intervention and Placebo Group Monitoring Chart were collected. The qualitative data obtained in the study were evaluated using descriptive and content analysis methods. Statistical Package for the Social Sciences program was used to evaluate the quantitative data. A value of p \< 0.05 will be accepted as statistical significance criterion. In order to carry out the study, the necessary Academic Committee decision, Ethics Committee approval (dated 11 November 2020 and numbered 13) and institutional permission were obtained. The individuals included in the study were informed about the purpose of the study.

Conditions

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Muscle Cramps Aromatherapy Hemodialysis Quality of Life Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Investigators

Study Groups

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Intervention group (Aromatherapy group)

With a mixture of Lavandula angustifolia, Rosmarinus officinalis L. and Origanum majorana L. essential oils, the foot and lower leg will be massaged for three sessions a week for 30 minutes in each session for four weeks.

Group Type EXPERIMENTAL

Lavandula angustifolia, Rosmarinus officinalis L. and Origanum majorana L.

Intervention Type OTHER

Massage application

Placebo group

The foot and lower leg will be massaged with baby oil for four weeks, three sessions a week, 30 minutes in each session.

Group Type EXPERIMENTAL

Baby oil

Intervention Type OTHER

Massage application

Control group

No application will be made in addition to standard HD treatment.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Lavandula angustifolia, Rosmarinus officinalis L. and Origanum majorana L.

Massage application

Intervention Type OTHER

Baby oil

Massage application

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Above 18 years old,
* Able to answer questions and communicate,
* Is conscious and does not have a mental problem,
* Speaks Turkish,
* No hearing, sight or speech impairment,
* Having HD treatment for at least six months,
* Receiving three HD treatment sessions a week,
* Dialysis with bicarbonate dialysate,
* Kt / V value\> 1.2,
* Having a constant dry weight for the last month,
* Experiencing cramps during hemodialysis sessions or at any other time and who scored at least three or more when the severity of cramp pain was evaluated with the Visual Analog Scale (VAS),
* Patients who are not allergic to the oils used for massage will be included in the study.

Exclusion Criteria

* Pregnant and breastfeeding women,
* Cancer,
* Diabetic foot,
* Lower extremity amputation,
* Having neurological diseases such as epilepsy, parkinson, dementia, Alzheimer,
* Those with paraplegia,
* The lower leg is in a size that prevents the application of massage,
* had surgery in the last three months,
* Loss of sensation more than 50% due to neuropathy due to various reasons,
* Open wound in the foot and lower leg, infection, necrosis, fracture / fracture suspected, soft tissue damage, burn,
* Peripheral vascular disease,
* Deep vein thrombosis,
* Receiving treatment to prevent cramping,
* Having a severe electrolyte (such as potassium, magnesium, calcium) disorder in blood values,
* Patients using any of the complementary and integrated methods in the last month will not be included in the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Serife Cetin

PhD student

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Serife Cetin, PhD

Role: PRINCIPAL_INVESTIGATOR

Kayseri University

Locations

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Erciyes University

Melikgazi, Kayseri, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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PhD student

Identifier Type: OTHER

Identifier Source: secondary_id

Erciyes University

Identifier Type: -

Identifier Source: org_study_id

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