Effects of Aromatherapy on the Headache and Service Quality Among Nurses Working in Critical Care Nurses Units.

Sponsor

National Taiwan University Hospital (Other)

Overall Status

Unknown status

CT.gov ID

NCT03867864

Collaborator

(none)

103

Enrollment

Arms

9.6

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Background: Our pilot study showed that the prevalence of headaches is 43.5% among nurses working in critical care units in a medical center in Taiwan. In the pilot study, 70% nurses with headache are willing to participate in this intervention study with essential oil. The effect of aromatherapy (essential oils through smelling) is convenient for nurses but still lacks strong evidences regarding relieving headaches.

Purpose: Thus, in this intervention study, we will examine whether the necklace with essential oil can (1) improve the pain intensity and frequency of headache; (2) reduce the score of headache disability inventory (HDI) and (3) improve the nurses' quality of life and care quality.

Method: Cluster randomized control trial from 16 critical care units at a medical center in Taiwan. The International Classification of Headache Disorders (ICHD, 3rd edition) was used to identify the headache type as "migraine" or "tension-type headache." We will recruit the nurses from 16 critical care units who has migraine or tension-type headache and cluster random assign (according to the ward unit) to group A and B. The intervention of necklace with essential oil will use to compare with the other group. According to power analysis and possible attrition rate, 103 nurses will be recruited. All participants will be asked to complete self-administrated questionnaires, including headache information questions, headache disability inventory (HDI), Migraine Specific Quality of Life Questionnaire version 2.1 (MSQv2.1), Copenhagen burnout inventory (CBI), Service Quality Scale (SERVQUAL), Intention to leave inventory (ITL), Depression, Anxiety and Stress Scale (DASS-21), Tasks Undone-13 (TU-13). The quantitative data will analyze by percentage, mean, standard deviation, chi-square test, and generalized estimating equation (GEE).

Expected outcomes and future implications: The aromatherapy (necklace with essential oil) can reduce the pain intensity, frequency, disability of headaches, as well as enhance nurses' quality of life and care quality.

Condition or Disease	Intervention/Treatment	Phase
Headache, Migraine Quality of Life	Device: Necklace with essential oil for the first 4 weeks Device: Necklace without essential oil for the first 4 weeks Other: Washout Device: Necklace with essential oil for last 4 weeks Device: Necklace without essential oil for last 4 weeks	N/A

Detailed Description

This study adopts an experimental design with cluster randomization based on the ward unit. Eligible subjects are diagnosed migraine or tension-type headache nurses who are working in the critical care units and also have nurse license. Before conducting this study, the study has been approved by the institutional review board (IRB). The researcher (co-PI) and research assistances will approach potential participants during the ward meeting and invite them to participate in the study. Potential participants would be informed of the study purposes and interventions process, and be assessed and confirmed their type of headache. After completing the written-informed consent, the interventions will be arranged. In order to control the quality of data collection, PI and co-PI have trained the research assistants. Research training included standardized research process and ethical concerns about collection of research data, methods of approaching eligible subjects, interviewing techniques of data collection.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

103 participants

Allocation:

Randomized

Intervention Model:

Crossover Assignment

Masking:

Single (Investigator)

Primary Purpose:

Other

Official Title:

Hao-Yuan Chang, Assistant Professor, School of Nursing, National Taiwan University

Anticipated Study Start Date :

Mar 15, 2019

Anticipated Primary Completion Date :

Dec 31, 2019

Anticipated Study Completion Date :

Dec 31, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Group A Group A participants will wear the necklace with essential oil for the first 4 weeks except take a shower or get to sleep. The participants will stop wearing the necklace for one week (the fifth week) for washout period, and then wear the necklace without essential oil for last 4 weeks (the sixth to ninth weeks).	Device: Necklace with essential oil for the first 4 weeks The necklaces contain essential oil. Other: Washout Washout (do not wear the necklace) for one week for two groups, then two groups cross-over. Device: Necklace without essential oil for last 4 weeks The necklaces do not contain essential oil.
Other: Group B The group B will wear the necklace without essential oil for the first 4 weeks except take a shower or get to sleep. The participants will stop wearing the necklace for one week (the fifth week) for washout period, and then wear the necklace with essential oil for last 4 weeks (the sixth to ninth weeks).	Device: Necklace without essential oil for the first 4 weeks The necklaces do not contain essential oil. Other: Washout Washout (do not wear the necklace) for one week for two groups, then two groups cross-over. Device: Necklace with essential oil for last 4 weeks The necklaces contain essential oil.

Arm

Intervention/Treatment

Experimental: Group A

Group A participants will wear the necklace with essential oil for the first 4 weeks except take a shower or get to sleep. The participants will stop wearing the necklace for one week (the fifth week) for washout period, and then wear the necklace without essential oil for last 4 weeks (the sixth to ninth weeks).

Device: Necklace with essential oil for the first 4 weeks

The necklaces contain essential oil.

Other: Washout

Washout (do not wear the necklace) for one week for two groups, then two groups cross-over.

Device: Necklace without essential oil for last 4 weeks

The necklaces do not contain essential oil.

Other: Group B

The group B will wear the necklace without essential oil for the first 4 weeks except take a shower or get to sleep. The participants will stop wearing the necklace for one week (the fifth week) for washout period, and then wear the necklace with essential oil for last 4 weeks (the sixth to ninth weeks).

Device: Necklace without essential oil for the first 4 weeks

The necklaces do not contain essential oil.

Other: Washout

Washout (do not wear the necklace) for one week for two groups, then two groups cross-over.

Device: Necklace with essential oil for last 4 weeks

The necklaces contain essential oil.

Outcome Measures

Primary Outcome Measures

Changes of Headache Diary [The participants will be assessed among pre-test week 1 (T1) and persistent to fill out the headache diary every day for 9 weeks (totally 63 days)]
The Headache Diary measured the participants to record the condition of headache with 12 items. The investigators will analyzed the intensity, frequency, duration, location, quality, symptoms, time and medicine use, and the duration (hours) of wearing the necklace with essential oil. At the meanwhile, we also collect the perceived busy level of the work day to control the association between the workload and headache. Thus, the participants have to write the diary everyday for 9 weeks and we will remind them by the text. The diary also mixes in the short-form McGill pain questionnaire (SF-MPQ) that was developed by Melzack in 1975 and revised in 1987 and it developed from the different type of headache depending on the pain intensity and quality (Melzack, 1975). The investigators simplified the contents and transfer to code so that the participants can easily fill out the diary every day.
Changes of Headache Disability Inventory (HDI) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Headache Disability Inventory (HDI) measured the burden caused by chronic headaches with 27 items (French et al., 2000). Each item scored from 1 to 3 (1= always happened; 3 = never happened). The higher score indicated the higher impacts of headache on emotional function and daily life.
Changes of Migraine Specific Quality of Life Questionnaire version 2.1 (MSQv2.1) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Migraine Specific Quality of Life Questionnaire version 2.1 (MSQv2.1) measured the quality of life of migraine and headache patients, including the function, limitation, burden and impacts of the migraine with 14 items (Bagley et al., 2011). Each item was scored from 1 to 6 (1= always happened; 6 = never happened). The higher score indicated the higher impact of headache on quality of life. Cronbach's alphas are 0.79-0.85 (Bagley et al., 2011).
Changes of Copenhagen Burnout Inventory (CBI) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Copenhagen Burnout Inventory (CBI) measured occupational burnout with 21 items (Yah et al, 2008). The questionnaire is including subscales-personal burnout, work-related burnout, client-related burnout, and over-commitment to work. Each item scored from 1 to 5 (1= never happened, 5 = always happened). The higher scores indicated the stronger work burnout. Cronbach's alphas are 0.89-0.95 (Yang et al, 2014).
Changes of Service Quality Scale (SERVQUAL) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Service Quality Scale (SERVQUAL) measured the care quality of nurses in the hospital, including the four domains: trustworthiness, responsiveness, promise and empathy with 28 Likert's scale items (Teng et al., 2007). Each item scored from 1 to 5 (1= strongly disagree; 5 = strongly agree). The higher score indicated the higher confidence on their care quality.
Changes of Intention to Leave Inventory (ITL) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Intention to Leave Inventory (ITL) measured the intention to leave the organization and their future career plan with 7 Likert's scale items (Teng, Shyu, & Chang, 2007). Each item scored from 1 to 7 (1= strongly disagree; 7 = strongly agree). The higher score indicated the higher strongly intention to leave the organization.
Changes of Depression, Anxiety and Stress Scale (DASS-21) [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The Depression, Anxiety and Stress Scale (DASS-21) measured the level of depression, anxiety and stress during the past week recently by 21 items (Moussa, 2001). Each item scored from 1 to 4 (1= strongly disagree; 4 = strongly agree). The higher score indicated more frequency of feeling depression, anxiety and stress (Lovibond & Lovibond, 2004). Cronbach's alphas were 0.87-0.94 (Black et al., 2015).
Demographic and Headache Information Questionnaire [The participants will be assessed at pre-test week 1 (T1)]
The Demographic Questionnaire included the birth date, sex, marital status, amenorrhea, education, unit, working years and rank. Although the necklace's colors are distributed randomly, considering the color may also affect the participants 'mood or the condition of headache, therefore, The investigators also survey the subject's preference of color to control the potential effect. The Headache Information Questionnaire was modified from the International Classification of Headache Disorders (ICHD, 3rd edition) to identify the headache type as "migraine" or "tension-type headache. Items included pain intensity, frequency, onset of the times, symptoms, locations, etc.
Tasks Undone-13 [The participants will be assessed among pre-test week 1 (T1), week 5 (T2) and week 10 (T3)]
The tasks undone-13 measured the missed care with 13 items (Aiken et al; Ball et al., 2013; Schubert, 2007). Each item scored from 0 to 1 (0 = left done, 1 = done and NA= not applicable) The higher score indicated the volume of care left done. Cronbach's alpha = 0.73 (Lucero et al., 2009) and content validity index is 0.70-0.91 (Squires et al., 2013)。

Eligibility Criteria

Criteria

Ages Eligible for Study:

20 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Registered nurses, working in intensive care units (ICU) or department of emergency (ED).
The frequency of headaches more than three times per month.
The type of headache is migraine or frequent episodic tension-type headache, which is defined by the Headache Classification Committee of the International Headache Society. If the symptoms of a headache cannot be defined, the investigator will refer the potential participant to a neurologist for further diagnosis.

Exclusion Criteria:

Current user of other kinds of essential oils (e.g., the external application on skin, sniffing), and do not willing to temporarily suspend for nine weeks.
Having sensitive responses to the essential oil.
Pregnancy or preparing for pregnancy.
Breastfeeding.
The type of headache was neither migraine nor frequent episodic tension-type headache after diagnosed by the neurologist.
With hepatic or renal diseases.
taking medicine for long-term (such as Aspirin, anti-coagulant, medication for mental disorders, contraceptives, etc.).