Eelderly With Sleep DisturbancesNCT06652789
Efficacy of Sleep Hygiene Intervention in Elderly With Insomnia
A study testing Sleep hygiene in people with Eelderly With Sleep Disturbances, run by University of Pittsburgh at 1 site in India.
Trial summary
Sleep disorders are common among elderly, especially among those with mental health disorders. Impaired quality of sleep, in elderly, can lead to worsening of mental and physical health too. Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Eelderly With Sleep Disturbances
- What is being tested?
- Sleep hygiene
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteIndia
- Study dates
- Feb 2027to 31 Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Elderly patients
- Age 60 years and above
- With self-reported sleep disturbances, scoring >5 on PSQI
- Who speak and understand one of English/ Kannada/ Hindi/ Tamil/ Telugu
Who cannot join
- With delirium
- With terminal medical illness
- Parkinsons disease, dementia
- Patients with severe mental illness
- Clinically diagnosed obstructive sleep apnea
- Patients who fulfil ICD-10 criteria for Alcohol Dependence syndrome
Show all 9Show fewer
- Patients who are on medications that interfere with sleep like hypnotics, anxiolytics, stimulants
- Patients who are on anti-depressants and antipsychotics
- Patients with restless leg syndrome.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
India1 site
St.John's Medical College and Hospital
Bengaluru, Karnataka, 560034
Smita Deshpande, MD
About this study
Official title: A Study to Evaluate the Efficacy of a Sleep Hygiene Behavior Intervention in Elderly With Insomnia
Sleep disorders are common among elderly, especially among those with mental health disorders. Impaired quality of sleep, in elderly, can lead to worsening of mental and physical health too. Due to high patient to doctor ratio in India and paucity of time in busy outpatients, there is inadequate information on causes of poor sleep quality in patients and a tendency to treat poor sleep with drugs. Studies on effectiveness of sleep hygiene techniques in insomnia also tend to exclude elderly. Thus, investigators have inadequate evidence on the applicability of such interventions in the elderly. In this study it is proposed to find the efficacy of a sleep hygiene behavioural intervention on severity of insomnia in elderly with sleep disturbances.
Read the detailed description
Globally, the older population is increasing rapidly, and between 2015 and 2050, it is expected that the proportion of the world's population over 60 years will nearly double, from 12% to 22% (World Health Organization 2022).Untreated insomnia and other sleep disorders can have major health consequences (e.g., cardiovascular and metabolic disease, impaired cognitive functioning, and increased risk of psychiatric disorders, as well as an increased risk of accidents Studies have also shown that poor sleep is associated with increased risk of falls in the elderly Poor sleep quality has been shown to be associated with decline in cognitive function, impaired quality of life (QOL), excessive daytime sleepiness, fatigue, depression, increased mortality, economic burden, and possibly early institutionalization.
Insomnia is defined as "difficulty initiating sleep, difficulty maintaining sleep, morning awakening, or sleep that is chronically non-restorative or poor in quality, associated with daytime impairment such as fatigue, memory impairment, social or vocational dysfunction, or mood disturbance." There are several objective and subjective assessment tools for measuring sleep disorders, among which polysomnography (PSG) is the gold standard. Considering the time-consuming nature of PSG, associated expense and poor availability of it to most clinicians, it is generally not routinely used in the assessment of insomnia.
Studies have shown that people with insomnia engage in specific poor sleep hygiene practices, which may perpetuate insomnia. However, studies examining the effect of sleep hygiene practices on insomnia, illness severity and cognition are lacking in elderly patients. Sleep hygiene techniques can serve as a relatively inexpensive lifestyle intervention in elderly patients with insomnia. Sleep hygiene recommendations may be delivered using a variety of media and measures (print based, in person discussions, telephonic conversations, etc), resulting in increased access. In addition to being commonly used and readily available, sleep hygiene education does not necessarily require the direct involvement of a clinician and therefore can be widely disseminated, even to elderly persons or their caregivers, who may not seek medical treatment for their sleep problems.
Estimated required sample size:
n1 = 43 n2 = 43 n1 + n2 = 86
Formula used:
Where, σ - Pooled standard deviation d - Difference between 2 group means Z1-β - Z value for corresponding power Z1-α/2 - Two-sided Z value for corresponding α (1.96)
Description of Intervention The intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period.
The 2 Direct face to face sessions will focus on health education about sleep. Each session will be conducted by a facilitator who has received training on the program, and will be delivered in a language that the participant is most fluent in (English/ Kannada/ Hindi/ Tamil/ Telugu). In case the participant is unable to come to the hospital for the session, the facilitator will visit the home of the patient to conduct the session (After taking consent).
- st face to face session (60 mins) Participants (and caregivers if available) will be informed about the study once again. Information will be given about lifestyles that can affect sleep positively or negatively- adequate sleep time required for health, healthy and unhealthy sleep habits Proper nutrition and fluid intake, exercise, smoking, alcohol habits and their relation to sleep will be discussed Common sleep myths will be covered briefly The consequences of poor sleep will be explained The sleep hygiene intervention will have 14 simple steps to be followed by participants- 1) Food/snacks have to be consumed at least 2 hours before bed time 2) Avoid electronic gadget usage i.e., mobile phone, laptop for at least 1 hour before bedtime 3) Go to bed only when feeling sleepy and not before 4) Using the bedroom only for sleep or sexual activity 5) Getting out of bed if unable to fall asleep 6) Avoid fluid intake 1 hour before bedtime 7) Avoid caffeine 4 hours before bedtime 8) Avoid Alcohol/Smoking 2 hours before bedtime 9) Lights should be turned off/to very dim immediately after going to bed 10) Avoid planning for next day or future activities on bed 11) Do not look at the time if the sleep is disturbed in between 12) Maintain regular sleep and wake up time with maximum of ½ hour deviation 13) Avoid noisy environment after going to bed (avoid discussion/arguments/ loud songs) 14) Avoid fasting Participants will be asked to rate their confidence level of following the above steps on a scale from 1 (not at all confident) to 10 (completely confident). If the participant's rating is below 7, they will be asked to discuss perceived barriers to following the steps, ways to overcome them and increase their confidence level to a rating of at least 7. Participants will be provided with a booklet containing all of the information covered in the first session.
- nd face to face session The session will start with participants being asked to summarize what they have learnt from the previous face to face session as well as weekly telephone calls Participants will be asked to indicate how many of the sleep hygiene techniques they were able to successfully implement since the previous session Successes and barriers faced during the previous month will be discussed. Facilitator will attempt to provide solutions for standard difficulties faced Participants will be reminded that not all recommendations may work for them. They will be encouraged to view the 6week period as an opportunity to discover approaches that will work for them personally.
Sleep hygiene techniques will be reiterated once again The session will also involve setting goals for the following 3 weeks based on performance during the previous month Twice a week telephone calls The participants will be followed up through telephonic conversation twice weekly with a gap of three to four days in between each call. Total 10 calls over 6-week period (only 1 call in the weeks where the face-to-face sessions are conducted, and this call will cover the points mentioned next under first call per week) Data Collection Tools A questionnaire including demographic characteristics and 6 standardized tools for assessment of sleep quality, depression, anxiety, cognitive status, quality of life, loneliness and pain severity will be used to collect the data for the study.
- Socio-demographic data sheet in elderly: Will include name, age, sex, address, religion, education, occupation, income, marital status, presence of any co-morbidities, presence of any substance use, diagnosed psychiatric illness, duration of illness, medications the patient is on, participant's co-morbidities, list of medications that the participant is on, average number of time participant wakes up to pass urine (developed by the researchers).
- Pittsburgh Sleep Quality Index (PSQI): The PSQI is a 19-item, self-rated questionnaire. It was developed by Buysse et al. to measure sleep quality and disturbance over the past month. It is intended to be used as a standardized sleep questionnaire in clinical settings. The 19 items are grouped into 7 components. Each of the sleep components is scored from 0 to 3, with 3 indicating the most dysfunction. The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality.
- The Montreal Cognitive Assessment (MoCA): The MoCA was designed as a rapid screening instrument for assessment of cognitive impairment. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.
- Patient Health Questionnaire 9 (PHQ-9): The PHQ-9 is the nine-item depression scale of the patient health questionnaire. The nine items of the PHQ-9 are based directly on the nine diagnostic criteria for major depressive disorder in the DSM-IV. The PHQ-9 can function as a screening tool, an aid in diagnosis, and as a symptom tracking tool that can help track a patient's overall depression severity as well as track the improvement of specific symptoms with treatment.
- Generalized Anxiety Disorder scale (GAD 7): The GAD-7 represents an anxiety measure based on seven items which are scored from zero to three. The whole scale score can range from 0 to 21 and cut-off scores for mild, moderate and severe anxiety symptoms are 5, 10 and 15 respectively.
- Short form of the revised UCLA Loneliness Scale: The scale consists of 3 items with response options hardly ever or never, some of the time and often. Responses to the items are summed to obtain the total scale score which ranges from 3 to 9 with higher scores indicating greater levels of loneliness (α = 0.72)
- WHO Quality of Life Brief Questionnaire (WHOQoL BREF): It consists of 24 items to assess perception of quality of life in four domains, including physical health, psychological, social relationships and environment, and two items on overall QOL and general health. A higher score indicated a better QOL.
- Visual Analogue Scale for Pain: The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."
- Conditions
- Eelderly With Sleep Disturbances
- Being tested
- Sleep hygiene
- Keywords
- Sleep hygiene, Elderly, sleep disturbances
- Medical subject headings
- Sleep Hygiene, Parasomnias
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Sleep hygieneBehavioural
The intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period.
The 2 Direct face to face sessions in local language will focus on health education about sleep. (After taking consent)
- st session (60 mins) Information will be given about lifestyles that can affect sleep positively or negatively- adequate sleep time required for health, healthy and unhealthy sleep habits
- nd session Participants will be asked to indicate how many of the sleep hygiene techniques they were able to successfully implement since the previous session Successes and barriers will be discussed. provide solutions for standard difficulties faced Twice a week telephone calls. The participants will be followed up through telephonic conversation twice weekly with a gap of three to four days in between each call.
| Study group | Role | What they receive |
|---|---|---|
| Sleep hygiene teaching | Experimental | The intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period.
The 2 Direct face to face sessions will focus on health education about sleep. Each session will be conducted by a facilitator who has received training on the program, and will be delivered in a language that the participant is most fluent in (English/ Kannada/ Hindi/ Tamil/ Telugu). In case the participant is unable to come to the hospital for the session, the facilitator will visit the home of the patient to conduct the session (After taking consent) Receives: Behavioral: Sleep hygiene |
What is being measured
The primary outcome is the main question the study is designed to answer.
Statistically significant change in PSQI score
Pre-and -post assessment by Pittsburgh Sleep Quality Index (PSQI).. The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality.
Measured: Baseline and after one month
Secondary outcomes (11)
Statistically significant change in PSQI score (Sustainability)
Pre-and -post assessment by Pittsburgh Sleep Quality Index (PSQI).. The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality.
Measured: Baseline and after three month
Changes of pertinent measures
measures on the actigraphy device at 1 month movement over time to assess sleep and wakefulness
Measured: Baseline and after one month
Changes of pertinent measures (sustainability)
measures on the actigraphy device at 3 months movement over time to assess sleep and wakefulness
Measured: Baseline and after three months
Statistically significant change in cognitive impairment measured by The Montreal Cognitive Assessment (MoCA )
The Montreal Cognitive Assessment (MoCA ) measures will be applied to measure cognive impairment. The Montreal Cognitive Assessment (MoCA) is a screening tool for mild cognitive impairment that's scored on a scale of 0 to 30 points. The total score is calculated by adding up the points from each task. A higher score indicates better cognitive function.
Measured: Baseline and after one months
Statistically significant change cognitive impairment (sustainability)
The Montreal Cognitive Assessment (MoCA ) measures will be applied to measure cognive impairment. The Montreal Cognitive Assessment (MoCA) is a screening tool for mild cognitive impairment that's scored on a scale of 0 to 30 points. The total score is calculated by adding up the points from each task. A higher score indicates better cognitive function.
Measured: Baseline and after three months
Statistically significant change in quality of life (WHO-QoL BREF score)
WHO Quality of Life Brief Questionnaire (WHOQoL BREF): It consists of 24 items to assess perception of quality of life . A higher score indicated a better QOL.
Measured: Baseline and after one month
Statistically significant change in quality of life (WHO-QoL BREF score) (Sustainability)
WHO Quality of Life Brief Questionnaire (WHOQoL BREF): It consists of 24 items to assess perception of quality of life . A higher score indicated a better QOL.
Measured: Baseline and after three month
Statistically significant change in pain
Visual Analogue Scale for Pain: The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain".
Measured: Baseline and after one month
Statistically significant change in pain (sustainability)
Visual Analogue Scale for Pain: The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain".
Measured: Baseline and after three month
Statistically significant change in Loneliness
Short form of the revised UCLA Loneliness Scale: The scale consists of 3 items with response options hardly ever or never, some of the time and often. Responses to the items are summed to obtain the total scale score which ranges from 3 to 9 with higher scores indicating greater levels of loneliness
Measured: Baseline and after one month
Statistically significant change in Loneliness (Sustainability)
Short form of the revised UCLA Loneliness Scale: The scale consists of 3 items with response options hardly ever or never, some of the time and often. Responses to the items are summed to obtain the total scale score which ranges from 3 to 9 with higher scores indicating greater levels of loneliness
Measured: Baseline and after three month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Oct 2024
- Study startFeb 2027 (estimated)
- Primary completionSep 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Eelderly With Sleep DisturbancesStudies of the same condition, open and under way.
- More trials run by University of PittsburghThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Proposed study design: Interventional study (Pre-post study design) Elderly Out-patient and in-patients of Psychiatry department, St. John's Medical College and Hospital, Bengaluru, and St. John's Community Health Centre, Mugalur
- Masking
- None (open label)
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Pittsburgh
- Sponsor type
- University, hospital or other
- Collaborators
- Fogarty International Center of the National Institute of Health
- Responsible party
- Principal investigator, Vishwajit Nimgaonkar, MD PhD, University of Pittsburgh
- Investigators
- Vishwajit L Nimgaonkar, MD, PhD, Principal investigator, University of Pittburgh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06652789
- Sponsor's protocol ID
- STUDY23120054
- Other IDs
- 5D43TW009114-10
- Status last verified
- Mar 2026
- First submitted
- 16 Oct 2024
- Last updated
- 27 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data collected during the trial as well as protocol will be shared on request at 1 years after results are published.
Study at a glance
From the registry record, last updated by the sponsor on 27 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Study to Evaluate the Efficacy of a Sleep Hygiene Behavior Intervention in Elderly With Insomnia
- ClinicalTrials.gov ID
- NCT06652789
- Acronym / sponsor ID
- STUDY23120054
- Conditions
- Eelderly With Sleep Disturbances
- Keywords
- Sleep hygiene, Elderly, sleep disturbances
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- University of PittsburghUniversity, hospital or other
- Collaborators
- Fogarty International Center of the National Institute of Health
- Study start
- Feb 2027 (estimated)
- Primary completion
- Sep 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 22 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Sleep disorders are common among elderly, especially among those with mental health disorders. Impaired quality of sleep, in elderly, can lead to worsening of mental and physical health too. Due to high patient to doctor ratio in India and paucity of time in busy outpatients, there is inadequate information on causes of poor sleep quality in patients and a tendency to treat poor sleep with drugs. Studies on effectiveness of sleep hygiene techniques in insomnia also tend to exclude elderly. Thus, investigators have inadequate evidence on the applicability of such interventions in the elderly. In this study it is proposed to find the efficacy of a sleep hygiene behavioural intervention on severity of insomnia in elderly with sleep disturbances.
Detailed description
Globally, the older population is increasing rapidly, and between 2015 and 2050, it is expected that the proportion of the world's population over 60 years will nearly double, from 12% to 22% (World Health Organization 2022).Untreated insomnia and other sleep disorders can have major health consequences (e.g., cardiovascular and metabolic disease, impaired cognitive functioning, and increased risk of psychiatric disorders, as well as an increased risk of accidents Studies have also shown that poor sleep is associated with increased risk of falls in the elderly Poor sleep quality has been shown to be associated with decline in cognitive function, impaired quality of life (QOL), excessive daytime sleepiness, fatigue, depression, increased mortality, economic burden, and possibly early institutionalization.
Insomnia is defined as "difficulty initiating sleep, difficulty maintaining sleep, morning awakening, or sleep that is chronically non-restorative or poor in quality, associated with daytime impairment such as fatigue, memory impairment, social or vocational dysfunction, or mood disturbance." There are several objective and subjective assessment tools for measuring sleep disorders, among which polysomnography (PSG) is the gold standard. Considering the time-consuming nature of PSG, associated expense and poor availability of it to most clinicians, it is generally not routinely used in the assessment of insomnia.
Studies have shown that people with insomnia engage in specific poor sleep hygiene practices, which may perpetuate insomnia. However, studies examining the effect of sleep hygiene practices on insomnia, illness severity and cognition are lacking in elderly patients. Sleep hygiene techniques can serve as a relatively inexpensive lifestyle intervention in elderly patients with insomnia. Sleep hygiene recommendations may be delivered using a variety of media and measures (print based, in person discussions, telephonic conversations, etc), resulting in increased access. In addition to being commonly used and readily available, sleep hygiene education does not necessarily require the direct involvement of a clinician and therefore can be widely disseminated, even to elderly persons or their caregivers, who may not seek medical treatment for their sleep problems.
Estimated required sample size:
n1 = 43 n2 = 43 n1 + n2 = 86
Formula used:
Where, σ - Pooled standard deviation d - Difference between 2 group means Z1-β - Z value for corresponding power Z1-α/2 - Two-sided Z value for corresponding α (1.96)
Description of Intervention The intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period.
The 2 Direct face to face sessions will focus on health education about sleep. Each session will be conducted by a facilitator who has received training on the program, and will be delivered in a language that the participant is most fluent in (English/ Kannada/ Hindi/ Tamil/ Telugu). In case the participant is unable to come to the hospital for the session, the facilitator will visit the home of the patient to conduct the session (After taking consent).
- st face to face session (60 mins) Participants (and caregivers if available) will be informed about the study once again. Information will be given about lifestyles that can affect sleep positively or negatively- adequate sleep time required for health, healthy and unhealthy sleep habits Proper nutrition and fluid intake, exercise, smoking, alcohol habits and their relation to sleep will be discussed Common sleep myths will be covered briefly The consequences of poor sleep will be explained The sleep hygiene intervention will have 14 simple steps to be followed by participants- 1) Food/snacks have to be consumed at least 2 hours before bed time 2) Avoid electronic gadget usage i.e., mobile phone, laptop for at least 1 hour before bedtime 3) Go to bed only when feeling sleepy and not before 4) Using the bedroom only for sleep or sexual activity 5) Getting out of bed if unable to fall asleep 6) Avoid fluid intake 1 hour before bedtime 7) Avoid caffeine 4 hours before bedtime 8) Avoid Alcohol/Smoking 2 hours before bedtime 9) Lights should be turned off/to very dim immediately after going to bed 10) Avoid planning for next day or future activities on bed 11) Do not look at the time if the sleep is disturbed in between 12) Maintain regular sleep and wake up time with maximum of ½ hour deviation 13) Avoid noisy environment after going to bed (avoid discussion/arguments/ loud songs) 14) Avoid fasting Participants will be asked to rate their confidence level of following the above steps on a scale from 1 (not at all confident) to 10 (completely confident). If the participant's rating is below 7, they will be asked to discuss perceived barriers to following the steps, ways to overcome them and increase their confidence level to a rating of at least 7. Participants will be provided with a booklet containing all of the information covered in the first session.
- nd face to face session The session will start with participants being asked to summarize what they have learnt from the previous face to face session as well as weekly telephone calls Participants will be asked to indicate how many of the sleep hygiene techniques they were able to successfully implement since the previous session Successes and barriers faced during the previous month will be discussed. Facilitator will attempt to provide solutions for standard difficulties faced Participants will be reminded that not all recommendations may work for them. They will be encouraged to view the 6week period as an opportunity to discover approaches that will work for them personally.
Sleep hygiene techniques will be reiterated once again The session will also involve setting goals for the following 3 weeks based on performance during the previous month Twice a week telephone calls The participants will be followed up through telephonic conversation twice weekly with a gap of three to four days in between each call. Total 10 calls over 6-week period (only 1 call in the weeks where the face-to-face sessions are conducted, and this call will cover the points mentioned next under first call per week) Data Collection Tools A questionnaire including demographic characteristics and 6 standardized tools for assessment of sleep quality, depression, anxiety, cognitive status, quality of life, loneliness and pain severity will be used to collect the data for the study.
- Socio-demographic data sheet in elderly: Will include name, age, sex, address, religion, education, occupation, income, marital status, presence of any co-morbidities, presence of any substance use, diagnosed psychiatric illness, duration of illness, medications the patient is on, participant's co-morbidities, list of medications that the participant is on, average number of time participant wakes up to pass urine (developed by the researchers).
- Pittsburgh Sleep Quality Index (PSQI): The PSQI is a 19-item, self-rated questionnaire. It was developed by Buysse et al. to measure sleep quality and disturbance over the past month. It is intended to be used as a standardized sleep questionnaire in clinical settings. The 19 items are grouped into 7 components. Each of the sleep components is scored from 0 to 3, with 3 indicating the most dysfunction. The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality.
- The Montreal Cognitive Assessment (MoCA): The MoCA was designed as a rapid screening instrument for assessment of cognitive impairment. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.
- Patient Health Questionnaire 9 (PHQ-9): The PHQ-9 is the nine-item depression scale of the patient health questionnaire. The nine items of the PHQ-9 are based directly on the nine diagnostic criteria for major depressive disorder in the DSM-IV. The PHQ-9 can function as a screening tool, an aid in diagnosis, and as a symptom tracking tool that can help track a patient's overall depression severity as well as track the improvement of specific symptoms with treatment.
- Generalized Anxiety Disorder scale (GAD 7): The GAD-7 represents an anxiety measure based on seven items which are scored from zero to three. The whole scale score can range from 0 to 21 and cut-off scores for mild, moderate and severe anxiety symptoms are 5, 10 and 15 respectively.
- Short form of the revised UCLA Loneliness Scale: The scale consists of 3 items with response options hardly ever or never, some of the time and often. Responses to the items are summed to obtain the total scale score which ranges from 3 to 9 with higher scores indicating greater levels of loneliness (α = 0.72)
- WHO Quality of Life Brief Questionnaire (WHOQoL BREF): It consists of 24 items to assess perception of quality of life in four domains, including physical health, psychological, social relationships and environment, and two items on overall QOL and general health. A higher score indicated a better QOL.
- Visual Analogue Scale for Pain: The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Proposed study design: Interventional study (Pre-post study design) Elderly Out-patient and in-patients of Psychiatry department, St. John's Medical College and Hospital, Bengaluru, and St. John's Community Health Centre, Mugalur
| Arm | Type | Receives |
|---|---|---|
| Sleep hygiene teaching | Experimental | Behavioral: Sleep hygieneThe intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period. The 2 Direct face to face sessions will focus on health education about sleep. Each session will be conducted by a facilitator who has received training on the program, and will be delivered in a language that the participant is most fluent in (English/ Kannada/ Hindi/ Tamil/ Telugu). In case the participant is unable to come to the hospital for the session, the facilitator will visit the home of the patient to conduct the session (After taking consent) |
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Elderly patients
- Age 60 years and above
- With self-reported sleep disturbances, scoring >5 on PSQI
- Who speak and understand one of English/ Kannada/ Hindi/ Tamil/ Telugu
Key exclusion criteria (9 listed)
- With delirium
- With terminal medical illness
- Parkinsons disease, dementia
- Patients with severe mental illness
- Clinically diagnosed obstructive sleep apnea
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Sleep hygieneThe intervention will be conducted over 6 weeks, and consist of engaging patients (and caregivers) in two 60-minute face to face sessions 3 weeks apart, and twice weekly telephonic follow ups lasting for 20 minutes each during the 6-week period. The 2 Direct face to face sessions in local language will focus on health education about sleep. (After taking consent) 1. st session (60 mins) Information will be given about lifestyles that can affect sleep positively or negatively- adequate sleep time required for health, healthy and unhealthy sleep habits 2. nd session Participants will be asked to indicate how many of the sleep hygiene techniques they were able to successfully implement since the previous session Successes and barriers will be discussed. provide solutions for standard difficulties faced Twice a week telephone calls. The participants will be followed up through telephonic conversation twice weekly with a gap of three to four days in between each call. | Behavioural | Sleep hygiene teaching |
Primary outcome
Statistically significant change in PSQI score
Time frame: Baseline and after one month
Pre-and -post assessment by Pittsburgh Sleep Quality Index (PSQI).. The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality.
11 secondary outcomes
Statistically significant change in PSQI score (Sustainability)
Time frame: Baseline and after three month
Changes of pertinent measures
Time frame: Baseline and after one month
Changes of pertinent measures (sustainability)
Time frame: Baseline and after three months
Statistically significant change in cognitive impairment measured by The Montreal Cognitive Assessment (MoCA )
Time frame: Baseline and after one months
Statistically significant change cognitive impairment (sustainability)
Time frame: Baseline and after three months
Statistically significant change in quality of life (WHO-QoL BREF score)
Time frame: Baseline and after one month
Statistically significant change in quality of life (WHO-QoL BREF score) (Sustainability)
Time frame: Baseline and after three month
Statistically significant change in pain
Time frame: Baseline and after one month
Statistically significant change in pain (sustainability)
Time frame: Baseline and after three month
Statistically significant change in Loneliness
Time frame: Baseline and after one month
Statistically significant change in Loneliness (Sustainability)
Time frame: Baseline and after three month
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Mar 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data collected during the trial as well as protocol will be shared on request at 1 years after results are published.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Vishwajit L Nimgaonkar, MD, PhD principal investigator
University of Pittburgh
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Sleep hygiene in people with Eelderly With Sleep Disturbances, run by University of Pittsburgh at 1 site in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 27 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Triptish Bhatia, PhD (09910107210, bhatiatriptish@yahoo.co.in), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Statistically significant change in PSQI score (time frame: Baseline and after one month). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Mar 2026.