Stress
Conditions
Keywords
mindfulness, meditation, internet
Brief summary
Phase 1 will follow 40 subjects and hopes to address whether or not IMMI can increase meditation practice as compared to another meditation program. The study will last six weeks for both the IMMI group (20 subjects) and the Access group (20 subjects). Access groups will receive learning materials and guided meditations, but the implementation will be self-paced. Participants in the IMMI group will receive weekly learning sessions and be required to practice meditation every day. IMMI group participants will also receive a weekly reminder call from a member of the study staff and have access to technical support in the event of trouble with the online program. All subjects will complete online self-report questionnaires that measure quality of life, self-efficacy, mood, sleep, mindfulness, and perceived stress at baseline and at the end of the six-week intervention. Subjects will also be given a questionnaire at the end of the study gauging their satisfaction with the mindfulness program they participated in. Phase 2 will follow 80 subjects and hopes to address whether or not IMMI is acceptable to participants and demographic information about IMMI users. The study will be the same as noted above, but all subjects will be entered in the IMMI program. Differences in recruitment rates, drop out, and patient satisfaction between the IMMI and Access groups will be analyzed. IMMI's ability to change meditation behavior (i.e. increasing time or frequency of meditation sessions), and improve quality of life will be examined as well.
Detailed description
Participants will undergo the following: Week 0 - Telephone screening; Week 1 - Baseline Assessment; Week 2-Week 7 - Internet Mindfulness Meditation Intervention (or Access in Phase 1); Week 8 - Endpoint Assessment
Interventions
BEHAVIORALInternet Mindfulness Meditation
BEHAVIORALAccess
Sponsors
Oregon Health and Science University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
* Age 18 - 80 years old * Access to Computer and Internet * Can hear and understand instructions * Willing to accept randomization scheme and agrees to follow the study protocol
Exclusion criteria
* Significant acute medical illness that would decrease likelihood of study completion (self-report) * Significant, untreated depression, as assessed by CESD-5 \>20 during screening * Current daily meditation practice (≥ 5 min/day daily for at least 30 days in the last 6 months. Past practice not exclusionary but will be recorded)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Enrollment rate | Week 0 - Screening | Number of participants who are eligible and enroll in the study |
| Participant satisfaction | Week 8 - Endpoint assessment | Client Satisfaction Questionnaire |
| Number of internet mindfulness meditation training sessions completed | Week 8 - Endpoint Assessment (after intervention is complete) | There are a total of 6 internet training sessions, and participants are instructed to complete one per week (where Week 0 is screening, Week 1 is Baseline Assessment, Week 2 is Training 1, Week 3 is Training 2, Week 4 is Training 3, Week 5 is Training 4, Week 6 is Training 5, and Week 7 is Training 6) . At the time of the endpoint assessment (Week 8), the number of completed training sessions is tabulated. |
| Completion Rate | Week 8 - Endpoint assessment | Number of participants who complete the endpoint assessment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mindfulness | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with Five Factor Mindfulness Questionnaire (FFMQ) |
| Quality of Life SF-36 | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with Short-Form Health Survey (SF-36) self-report measure |
| Perceived Stress | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with perceived stress scale (PSS) |
| Self-efficacy | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with General Perceived Self Efficacy (GPSE) self-report questionnaire |
| Mood | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with Center for Epidemiological Studies Depression Scale (CESD) self-report questionnaire |
| Sleep | Week 1 - Baseline assessment & Week 8 - Endpoint assessment | Measured with Pittsburgh Sleep Quality Index (PSQI) self-report questionnaire |
Outcome results
None listed