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Effect of massage on the level of anxiety

Comparison between aromatherapy message and foot reflexology on anxiety, depression, fatigue and hemodynamic parameters in hospitalized elderly women with acute coronary syndrome.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201512027529N8
Enrollment
135
Registered
2016-01-09
Start date
2015-05-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute coronary syndrome. Ischaemic heart diseases

Interventions

Intervention 1: Reflexology group :the researcher is washing hands with warm water and sit on the chair beside the patient. Then she is filling the scales (HADS, Roten Fatigue Scale, hemodynamic param
Reflexology group :the researcher is washing hands with warm water and sit on the chair beside the patient. Then she is filling the scales (HADS, Roten Fatigue Scale, hemodynamic parameters) and perfo
Aromatherapy massage group: the message will be the same as the first intervention with the difference that lavender essential oil is used during the message

Sponsors

Vice chancellor for research Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients’ willingness to participate in this study; Being diagnosed with the acute coronary syndrome by the physician; the absence of any cognitive impairment or impaired cognitive function in the patients; no application of alternative therapies in the past 48 hours; not using sedatives in the last 4 hours; having no olfactory disorders; the absence of any active mental disease; having no drug addiction; being hospitalized for at least one night in the current hospital; having no sensory disorders, infectious wounds, burns; having no history of asthma; eczema; allergies to plants or any seasonal allergy; suffering from no chronic headaches, high levels of anxiety and depression according to the HADS instrument (score higher than 7). Exclusion criteria: instability in the hemodynamic conditions; being transferred to another ward; patient’s unwillingness to continue the collaboration in this study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: HADS questionnaire.;Depression. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: HADS questionnaire.;Fatigue. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: Fatigue Severity Scale.;Blood pressure. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: Checklist.;Respiratory rate. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: Checklist.;Pulse rate. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: Checklist.;Oxygen saturation. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: pulse oximeter.;Mean blood pressure. Timepoint: Before the intervention in first session and in final any sessions. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nahid Rejeh

Shahed University

nrejeh@yahoo.com+98 21 5121 3071

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026