Investigate the effect of Rose esence on the sleep quality of hemodialysis patients

The effectiveness and ineffectiveness of Rose esence on the sleep quality of hemodialysis patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015110214333N45

Enrollment

Registered

2016-02-15

Start date

2016-01-20

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

hemodialysis. Extracorporeal dialysis

Interventions

Intervention 1: Experimental group will use 3 drops of Rose esence 10%, every night before bed for a month. Patients and attendants will trained, while using spills 3 drops of Rose esence on a cotton

Treatment - Drugs

Placebo

Experimental group will use 3 drops of Rose esence 10%, every night before bed for a month. Patients and attendants will trained, while using spills 3 drops of Rose esence on a cotton ball into a lay

In the control group will used sesame oil as a placebo.

Eligibility

Sex/Gender

All

Age

15 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age between 15 to 70 years; Patient informed consent; Patients undergoing hemodialysis; At least 6 months history of dialysis at a rate of 1 to7 times a week; Lack of Allergic Diseases Exclusion criteria: A score less than 5 of Pittsburgh Sleep Quality scale; Failure to perform systematic interventions for one third of intended time.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Subjective sleep quality. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire.;Sleep latency. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Duration of sleep. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Sufficient sleep. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Sleep disturbances. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).	—

Measure

Time frame

Subjective sleep quality. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire.;Sleep latency. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Duration of sleep. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Sufficient sleep. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).;Sleep disturbances. Timepoint: Base line and end of the study (one month after the beginning of the study). Method of measurement: By Pittsburgh Sleep Quality questionnaire(PSQI).

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Countries

Iran (Islamic Republic of)

Outcome results

None listed

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