Effects of Aromatherapy on Sleep Quality in Hospitalized Elderly Female Patients With Insomnia

ConditionInsomnia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age60-100
SponsorThe Second Hospital of Anhui Medical University

About this trial

To evaluate the efficacy and safety of standardized aromatherapy compared with placebo in improving sleep quality among hospitalized elderly female patients with insomnia.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Female, aged ≥60 years.

Hospitalized in the Second Affiliated Hospital of Anhui Medical University.

Athens Insomnia Scale (AIS) >6.

Ability to communicate and understand instructions.

Disqualifiers

Cognitive impairment-.

History of hypersensitivity to aromatherapy oils.

Use of sedative-hypnotic medications within past 2 weeks.

Sleep disorders secondary to organic or psychiatric diseases.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Aromatherapy

    Other intervention

    Verify patient identity and explain the intervention. Ensure comfortable supine or semi-recumbent position. Drop 2 drops of lavender essential oil onto a sterile cotton ball; place inside disposable urine cup. Position cup 20 cm from patient's nostrils; instruct patient to perform 10 deep breaths. Place cup at bedside until morning. Lay treatment cloth under patient's wrists. Apply 1 drop of lavender oil to both thumbs, perform bilateral Shenmen (HT7) acupoint pressure on the wrist Shenmen acupoint pressure for 10 minutes per side, moderate pressure causing mild local distension but no pain. Restore patient to comfortable position; remove materials; wash hands. Record any immediate reactions or discomfort.

  • Placebo

    Other intervention

    Identical procedure using odorless fractionated coconut oil. Sham acupoint pressure on a non-acupoint location near the wrist performed identically to maintain blinding.

Treatment groups

64 Participants
are divided into 2 treatment groups
Group A: aromatherapyExperimental treatment 1 intervention
Group B: placeboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Athens Insomnia Scale

Total score 0-24; higher scores indicate worse insomnia.

Time frame
Evaluated at baseline, day 6 and 2-week follow-up.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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