Step-2-It: Feasibility of SMS Technology to Increase Physical Activity (Step-2-It)
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| ClinicalTrials.gov Identifier: NCT04812756 |
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Recruitment Status :
Completed
First Posted : March 24, 2021
Last Update Posted : March 24, 2021
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Rural women are more likely to be obese and have a higher risk for chronic disease than their non-rural counterparts. Inadequate physical activity (PA) at least in part contributes to this increased risk. Rural women face personal, social and environmental barriers to PA engagement. Interventions promoting walking among rural women have demonstrated success; however, few of these studies use text messaging to promote PA.
Step-2-It was a pilot study to assess the feasibility, acceptability, and effectiveness of text-messaging combined with a pedometer to promote PA, specifically walking among English-speaking women, aged 40 and older, living in a rural, northwest Illinois county. There were two components to the 13-week, Step-2-It intervention: (i) participants used the pedometer to track and report their steps via text message daily; and (ii) participants received an informational or motivational text message daily. Enrolled participants completed baseline assessments, received pedometers and two types of automated text messages: motivational messages to encourage walking, and accountability messages to report pedometer steps. Participants engaged in 3, 6, 9, and 12-week follow-ups to download pedometer data, and completed post-intervention assessments at 12 weeks.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Health Behavior | Behavioral: Step-2-It - text messaging program | Not Applicable |
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| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 44 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Intervention Model Description: | Single group prospective pre-post study |
| Masking: | None (Open Label) |
| Primary Purpose: | Other |
| Official Title: | Step-2-It: A Pilot Study to Assess Feasibility of Using SMS Based Mobile Technology to Increase Physical Activity in Adult Rural Women at Risk for Cardiovascular Disease |
| Actual Study Start Date : | August 15, 2014 |
| Actual Primary Completion Date : | February 15, 2015 |
| Actual Study Completion Date : | June 15, 2016 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Texting intervention
This is a single arm study in which all participants received a pedometer and text messages for the 12 week intervention period. Participants received a content message and a message requesting them to report the number of steps from their pedometer daily.
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Behavioral: Step-2-It - text messaging program
participants received a pedometer and text messages to motivate them to increase walking daily for a period of 12 weeks. |
- Physical Activity levels [ Time Frame: Change from baseline to end of intervention at 12 weeks ]mean steps per day measured using pedometer
- Physical Activity Levels [ Time Frame: Change from baseline to end of intervention at 12 weeks ]PA measured via self-report using the BRFSS PA tool
- Body-weight [ Time Frame: Change from baseline to end of intervention at 12 weeks ]Body weight measured using a calibrated scale
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| Ages Eligible for Study: | 40 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Women
- Age 40 and older
- Reside in Stephenson County
- Own a cell phone with ability to receive and send text messages
- Unlimited texting plan
- Able to give informed consent
- Speak English
Exclusion Criteria:
- Men
- Women under 40 years of age
- Reside outside Stephenson County
- No cell phone or no texting ability
- Non-English speaking
- Unable to provide informed consent
- Significant health conditions (including pyelonephritis, current treatment for cancer, other severe illness)
- Active severe asthma
- Current pneumonia
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04812756
| Principal Investigator: | Manorama M Khare, PhD | University of Illinois College of Medicine Rockford |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | University of Illinois College of Medicine Rockford |
| ClinicalTrials.gov Identifier: | NCT04812756 |
| Other Study ID Numbers: |
622085-5 |
| First Posted: | March 24, 2021 Key Record Dates |
| Last Update Posted: | March 24, 2021 |
| Last Verified: | March 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

