Insomnia Clinical Trial
Official title:
Impact Of Mindfulness Breathing Versus Storytelling On Non- Specific Insomnia In Elderly
This study will be conducted to compare between effects of mindfulness breathing and storytelling on insomnia in the elderly.
Status | Recruiting |
Enrollment | 93 |
Est. completion date | April 2024 |
Est. primary completion date | March 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years and older |
Eligibility | Inclusion Criteria: - Patients who have non-specific insomnia for one month at least. - Their ages > 65 years. - Medically stable patients. - Current complaint of poor SQ (score > 5 of the SQ scale) - Body mass index = 35 kg/m2. Exclusion Criteria: - Patients having a well-structured diagnosis of relevant brain illness or - any disease directly affects sleep. - Any patient with unstable medical condition - History of chronic insomnia - Indication of receiving treatments for depression and anxiety - Hearing problem |
Country | Name | City | State |
---|---|---|---|
Egypt | Naser specialized hospital | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Pittsburgh Sleep Quality Index | Pittsburgh Sleep Quality Index (PSQI) as a valid tool was used to measure the patients' SQ. This instrument was comprised of seven domains, including quality of subjective sleep, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, daytime dysfunction, and use of medication for sleep over the previous month. The score of the domains ranged from 0 = "No difficulty" to 3 = "Severe difficulty". A total score > 5 was considered to be indicative of poor SQ. A global score between 0 and 21 was derived by summing up the seven subscale scores | baseline | |
Primary | Actigraphy | Actigraph (Actiwatch Minimitter Company, INC - Sunriver, OR, USA) will be placed on the non-dominant wrist and activities will be monitored continuously and recorded at one minute intervals during wakefulness and sleep.
The times of wakefulness and sleep will be determined individually through a diary kept by the volunteers, together with the times calculated by the actigraph monitor. The participants will keep the device for a period of 7 days before the first and the last training session. The device will be removed only at bath time and replaced to the wrist immediately after. The information will be collected by the device and recorded by a validated algorithm (Minimitter Company - USA®) and transferred to a closed technology software installed on a computer. After analysis of the exams, the data will be plotted on a spreadsheet for statistical treatment |
baseline |
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