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Reflexology Versus Acupressure on Sleep Disturbance and Hot Flashes

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Hot Flashes
Postmenopausal Flushing

Treatments

Other: Acupressure
Other: Foot Reflexology

Study type

Interventional

Funder types

Other

Identifiers

NCT06499311
REC/012/005081

Details and patient eligibility

About

World health Organization (WHO) estimates that by 2030, 1.2 billion women will be over 50 years old. With a prevalence of 70%, a hot flash is the most distressing symptoms associated with menopause. Postmenopausal associated sleep disturbances could affect those women social activities and one's daily positive functioning. Therefore, some patients and their providers seek alternative treatments such as relaxation techniques, acupressure, yoga, reflexology, regular exercise, balanced nutrition, herbal supplements, appropriate clothing, and frequent showers, have been shown to be effective in reducing symptoms associated with depression. So, this study will be the first one in this issue. Therefore, it will have valuable benefits in physical therapy field and scientific research.

Full description

Fifty-four postmenopausal women suffering from moderate to severe hot flashes diagnosed with hot flashes questionnaire, and sleep disturbances diagnosed with Pittsburgh quality sleep index >5. Their age ranged from 45-55 years old with their body mass index ranged from 25 to 30 kilogram per meter square. Outcome measures were Pittsburgh sleep quality index and Hot flashes questionnaire, both were conducted at baseline and after the end of the study program. after recruiting study population, they will be divided into two equal groups randomly. Group A; will received foot reflexology (medical border just above the heel, reflex points associated with adrenal, hypothalamus, pituitary glands, heart and lung via manual pressure at reflexology zone), for 15 minutes, 3 sessions per week for 6 weeks. Group B; will received acupressure ((Shenmen point, Sanyinjiao point, Fengchi point; Yintang point), for 21 minutes, 3 sessions per week for 6 weeks.

Enrollment

54 estimated patients

Sex

Female

Ages

45 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ranged from 45 to 55 years old.
  • Their body mass index ranged from 25 to 3 kilograms per meter square.
  • Postmenopausal women suffering from moderate to sever hot flashes assessed by Hot Flashes Questionnaire.
  • Postmenopausal women suffering from sleep disturbances more than five assessed by Pittsburgh sleep quality index.

Exclusion criteria

  • Any emotional stress during at least 6 months.
  • Any pharmacological medicines lead to sleep disturbances.
  • Any mental disorders affect their sleep cycle.
  • Taking hormone replacement therapy for the past six months.
  • Using herbal medicine to improve menopausal symptoms severity.
  • Circular job in particular night shifts.
  • Sensorineural problems in their feet.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

54 participants in 2 patient groups

Group A; Foot Reflexology
Experimental group
Description:
Foot reflexology for 15 minutes, 3 sessions per week for 6 weeks will applied at the medical border just above the heel, also at associated reflex points associated with the adrenal, hypothalamus, pituitary glands, heart and lung via manual pressure at reflexology zone.
Treatment:
Other: Foot Reflexology
Group B; Acupressure
Experimental group
Description:
Acupressure for 21 minutes, 3 sessions per week for 6 weeks will applied at four acupoints points (Shenmen point at wrist crease, Sanyinjiao point; at both feet, and Fengchi point; at hairline within occipital region on dorsal neck surface), bilaterally in addition to one in midline at the top of nose on centerline between eyebrows ends (Yintang point).
Treatment:
Other: Acupressure

Trial contacts and locations

1

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Central trial contact

Elham S Hassan, PHD; Dr Mohamed A Awad, PHD

Data sourced from clinicaltrials.gov

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