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Efficacy of Automated Text Messaging Services

Efficacy of Automated Text Messaging Services on Sleep Health, Stress, Pain, and Function in Physical Therapy Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05621265
Enrollment
20
Registered
2022-11-18
Start date
2021-10-01
Completion date
2022-05-01
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Therapy, Sleep

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.

Interventions

BEHAVIORALAutomated Text messaging

daily text message

Sponsors

Black Hills State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adults 18 years and older seeking outpatient Physical Therapy

Exclusion criteria

Inability to access a smart-phone or computer

Design outcomes

Primary

MeasureTime frameDescription
Pittsburgh Sleep Quality Indexinitial visit and 4-week follow upsleep quality measurement. Scores range 0-21 with higher score indicating poorer sleep quality.
Sleep Hygiene Indexinitial and 4-week follow upmeasuring participants sleep hygiene behaviors. Scores range 0-52 with a higher score indicating poorer sleep hygiene.

Secondary

MeasureTime frameDescription
Perceived Stress Scaleinitial and 4-week follow upstress measurement. Scores range 0-40 with higher score indicating greater stress.
Patient Specific Functional Scaleinitial and 4-week follow upscale for improving patient's top three chosen functions they want to improve. Scores range from 0-10 with lower scores indicating poorer function.
Numeric Pain rating ScaleInitial and 4-week follow uptool to measure pain. 0-10 with 10 being highest pain possible.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026