Efficacy of Automated Text Messaging Services on Sleep Health, Stress, Pain, and Function in Physical Therapy Patients
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Black Hills State University
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Sleep Hygiene Index
Study Overview
Brief Summary
The goal of this clinical trial is to test automated text messaging as an effective behavior change intervention in physical therapy patients. The main purpose of this study was to trial sleep hygiene education for improving physical therapy patients' sleep through the use of daily automated text messaging. Researchers will compare two groups to see if the intervention group which consisted of participants getting daily automated text messages for sleep hygiene tips would be effective in improving sleep, health, pain, and function compared to a group that is receiving traditional physical therapy alone.
Detailed Description
Participants will be recruited from the outpatient physical therapy clinic verbally by their therapist and by an informational handout they receive from the therapist. The student researcher (who also works at this clinic) will then contact the participant to set up a time to complete the initial survey questions at the clinic in a private treatment room. During the initial visit, participants will read through and sign informed consent explaining the procedures and expectations of them during the study. The participants will then complete the following questionnaires: Pittsburgh Sleep Quality Index, Sleep Hygiene Index, Medical Outcome Survey-sleep 9, Perceived Stress Scale, Numeric Pain Rating Scale, and Patient Specific Functional Scale. The participants will randomly be assigned to one of two groups. The intervention group will receive daily automated text messages scheduled for 8:00 pm every evening. The text messages will include a variety of sleep hygiene behavioral tips for the participant to try. This will last for a total of four weeks. The control group will not receive any intervention during this time frame. Following the four weeks, student researchers will return to each participant's clinic to collect the same data that was collected at the initial visit. Each participant will have a total of 2 sessions to complete with each session taking approximately 15-30 minutes to complete.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adults 18 years and older seeking outpatient Physical Therapy
Exclusion Criteria
- •Inability to access a smart-phone or computer
Arms & Interventions
Intervention
Automated Text messaging for sleep behavior change
Intervention: Automated Text messaging (Behavioral)
Control
Control, Traditional physical therapy only
Outcomes
Primary Outcomes
Sleep Hygiene Index
Time Frame: initial and 4-week follow up
measuring participants sleep hygiene behaviors. Scores range 0-52 with a higher score indicating poorer sleep hygiene.
Pittsburgh Sleep Quality Index
Time Frame: initial visit and 4-week follow up
sleep quality measurement. Scores range 0-21 with higher score indicating poorer sleep quality.
Secondary Outcomes
- Perceived Stress Scale(initial and 4-week follow up)
- Patient Specific Functional Scale(initial and 4-week follow up)
- Numeric Pain rating Scale(Initial and 4-week follow up)