STRIDE: Stress Reduction in Dementia Caregivers

Caregiver Stress Clinical Trial

Official title:

Using Mobile Technology to Reduce Stress in Caregivers of Persons With Dementia. A Scalable Solution to a Growing Problem.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05732038
• Other study ID #: 2022P001601
• Status: Active, not recruiting
• Phase: N/A
• Start date: February 20, 2023
• Est. completion date: May 15, 2024

Study information

• Verified date: January 2024
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators aim to conduct a feasibility, proof of concept randomized controlled trial (RCT) of a smartphone app intervention (Healthy Minds Program; HMP) versus Wellness app (WA) among heterogeneous stressed caregivers of individuals with Alzheimer's disease and related dementias (ADRD). The investigators will test its feasibility (primary outcomes) and its preliminary effect in improvement in caregiver stress, emotional distress (depression and anxiety), sleep, and mindfulness. Participants will be randomized to one of the two conditions described above

Description:

Using the NIA 2 year R21 grant mechanisms, we will examine the feasibility (markers of acceptability and demand), and proof of concept of Healthy Minds Program (HMP) versus Wellness App (WA) in decreasing stress, emotional distress and sleep dysfunction in heterogeneous, geographically diverse, stressed caregivers of individuals with Alzheimer's disease and related dementias (ADRD). Participants in each arm will be asked to practice for 10 min/day. To achieve our aims, we will conduct a single blind, pilot, feasibility, proof of concept randomized controlled trial (RCT) of HMP (12 weeks, > 10 minutes daily) versus WA; 12 weeks, >10 minutes daily). Assessments will be conducted at baseline, post program (12 weeks later) and at 20 weeks follow-up (~2 months after post-test). Caregivers will also complete weekly assessments.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 93
• Est. completion date: May 15, 2024
• Est. primary completion date: May 15, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. 18 years or older

2. English fluency and literacy

3. Meeting criteria for being a caregiver (e.g., family or friend of a care recipient who provides unpaid care)

4. Perceived Stress Scale (4 items) version >= 6

5. Willing to be randomized

6. Care recipient must score >1 on the functional assessment scale (FAST)

Exclusion Criteria:

1. Any planned change in psychotropic pharmacologic treatment for the duration of the study

2. Use of any consumer-based mindfulness meditation app for more than 60 min/month in the past 6 months.

3. Current participation in a meditation program (e.g., mindfulness-based stress reduction, mindfulness-base cognitive therapy, etc.)

4. Major illness known to worsen dramatically or require surgery in the next 20 weeks (study duration)

5. Active treatment for cancer (chemotherapy, radiation)

6. Imminent placement of care recipient in a nursing home or with another caregiver (within 4 months).

7. Involvement in another clinical trial for caregivers.

8. For participants age 65 and older: four or more errors on the Short Portable Mental Status questionnaire (SPMSQ)

Related Conditions & MeSH terms

• Caregiver Stress
• Dementia

Intervention

Behavioral:
• Healthy Minds Program (HMP)
Participants assigned to the HMP group will be asked to complete a minimum of 10 minutes per day of meditation for 12 weeks. For the first four weeks, participants will listen to prescribed meditations that will teach them the foundations of mindfulness. During weeks 5-12, participants will have full access to the HMP meditation library.
• Wellness App (WA)
Participants in the WA group will listen to a minimum of 10 minutes per day of a caregiver specific educational podcast (including topics such as "Caring for the Caregiver" or "Folate and Preventing Alzheimer's") delivered via a mobile app for the 12 weeks. The app contains one podcast per day for twelve weeks.

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of Recruitment	We will assess number of dementia caregivers enrolled from the number of caregivers that were eligible. Our primary aim focuses on feasibility of recruitment during the trial.	0 weeks
Primary	Adherence to one of the two apps	We will assess data from the Healthy Minds Program app and the Podcast app to measure adherence to the intervention and the control conditions. Our benchmark will be that >=70% of caregivers will complete >=75% of weekly prescribed minutes (>=10 minutes/day).	12 weeks
Primary	Credibility and Expectancy Questionnaire (CEQ)	We will use the Credibility and Expectancy Questionnaire (CEQ) to assesses caregivers perceptions that the treatment will work after learning about the study. Scores range from 3-27; higher ratings indicate more belief that the program is logical and will help with the intended outcome.	0 weeks
Primary	Client Satisfaction Questionnaire (CSQ-3)	This will be used to assess caregivers' satisfaction with the intervention. Scores range from 3 to 12, with higher values indicating higher satisfaction.	12 weeks
Primary	Perceptions of daily meditations/podcast	We will assess caregivers' perception of their app's prescription by asking, "Do you think that the amount of daily prescribed app content was: too little, just enough, or too much?"	12 weeks
Primary	Perceptions of emails and text reminders	We will assess caregivers' perception of emails and text message reminders by asking, "Do you think that the amount of emails/texts you received was: too little, just enough, too much?"	12 weeks
Primary	Perceptions of the overall study	We will assess caregivers' perceptions of the study by asking, "Do you have any feedback about your experience in this program (content of the program, content of the text message reminders, etc.) that you would like to share?"	12 weeks
Primary	Feasibility of weekly Research Electronic Data Capture (RedCAP) measures	We will assess the feasibility of the weekly REDCap measures sent to patients by review of responses to ensure that >=70% caregivers will answer >=75%.	12 weeks
Primary	Perceptions of prompts/contacts in low adherence situations	We will assess caregivers' perception of the amount of prompts and contact in situations where they were not adhering to their practice by asking "Do you think that the amount of prompts you received when you struggled with your practice was: too little, just enough, too much?"	12 weeks
Primary	Feasibility of quantitative measures	We will assess the feasibility of the quantitative measures sent to caregivers with the benchmark of no questionnaires missing fully in >=25% caregivers.	20 weeks
Secondary	Hospital Anxiety and Depression Scale (HADS)	We will use the Hospital Anxiety and Depression Scale HADS, a 14-item measure that assesses symptoms of emotional distress (anxiety and depression). The anxiety and depression sub-scale are each scored from 0-21, with higher scores indicating greater severity of symptoms. Scores can be summed to create a global emotional distress score (0-42).	0 weeks, 12 weeks, 20 weeks
Secondary	Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance Short Form - 8 item	We will use the PROMIS sleep disturbance short form to assess caregivers' sleep. Each item is rated on a 5-point scale with the overall score ranging from 8 to 40. Higher scores indicate greater severity of sleep disturbance.	0 weeks, 12 weeks, 20 weeks
Secondary	Applied Mindfulness Process Scale (AMPS)	We will use the Applied Mindfulness Process Scale (AMPS) to assess caregivers mindfulness. AMPS consists of 3 sub scales: de-centering, positive emotion regulation, and negative emotion regulation. Each sub scale is scored from 0-20. An overall score ranging from 0-60 can be obtained by summing all 15 items. Higher scores indicate greater mindfulness.	0 weeks, 12 weeks, 20 weeks
Secondary	Stress Thermometer	We will use a stress thermometer scale (0-10) to assess how caregivers rate their level of stress each week: "During the past week, how would you rate your stress on a scale from 0-10? (0 = not at all; 10 = extremely stressed)?"	0-12 weeks, 20 weeks
Secondary	Sleep Thermometer	We will use a sleep thermometer scale (0-10) to assess quality of sleep: "During the past week, how would you rate your quality of sleep on a scale from 0-10? (0 = extremely low quality; 10 = extremely high quality)?"	0-12 weeks; 20 weeks
Secondary	Mindfulness Thermometer	We will use a mindfulness thermometer scale (0-10) to assess how caregivers rate their level of mindfulness each week: "During the past week, how would you rate your mindfulness on a scale from 0-10? (0 = not at all; 10 = extremely mindful)?"	0-12 weeks, 20 weeks
Secondary	Emotional Distress Thermometer	We will use an emotional distress thermometer scale (0-10) to assess how caregivers rate their level of distress each week: "During the past week, how would you rate your emotional distress on a scale from 0-10? (0 = not at all; 10 = extremely emotionally distressed)?"	0-12 weeks, 20 weeks
Secondary	Modified Patient Global Impression of Change (MPGI)	We will use the Modified Patient Global Impression of Change (MPGI), a 1-item questionnaire, to assess the extent to which caregivers perceive the intervention improved functioning and symptoms: "Do you think your ability to manage stress associated with caring for your loved one with dementia is now improved, about the same, or worse, as compared to before your participation in this program?"	12 weeks
Secondary	Perceived Stress Scale 10 items (PSS-10)	We will use the PSS-10, to assess perceived stress using a 5-point Likert scale. Scores range from 0 to 40 with higher scores indicating greater stress.	0 weeks, 12 weeks, 20 weeks
Secondary	Healthy Minds Index	This is a 17-item measure (each item is scored on a 0-4 scale) that assesses awareness (items 1-4; scored from 0-16), connection (items 5-10; scored from 0-24), insight (items 11-13; scored from 0-12), and purpose (items 14-17; scored from 0-16). Higher scores indicate greater levels of each sub scale.	0 weeks, 12 weeks, 20 weeks
Secondary	Caregiver Reaction Scale	This measure assesses caregiver burden. We are administering the following sub scales: role entrapment (4 items); role overload (4 items); mastery as a caregiver (4 items); self mastery (4 items); workplace productivity (5 items). Each item is measured on 1-4 point scale. Sub scales with 4 items are scored from 4-16; sub scales with 5 items are scored from 5-20. Higher scores indicate higher levels of each sub scale's construct.	0 weeks, 12 weeks, 20 weeks