Short Message System (SMS)
BehavioralThe Short Message System (SMS) intervention focuses on personalized, adaptive SMS messages that help the participant maintain physical activity behaviors.
Other names: SMS, Short Message Service
NCT Number: NCT06745180
The aim of this project is to help increase physical activity maintenance in cancer survivors.
Interested in participating?
Request Info19 year and older
Female
Interventional
Not applicable
University of Alabama at Birmingham, Birmingham, Alabama, United States
The purpose of the study is to evaluate novel interventions designed to assist women cancer survivors, who identify as African American or Black, in overcoming exercise barriers, developing a physically active mindset, and establishing exercise habits needed to exercise long term. These novel interventions are 1. Text Messaging (SMS), 2. Peer Coaching, 3. Combination of Peer Coaching and SMS, 4. Usual Care
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Short Message System (SMS) intervention focuses on personalized, adaptive SMS messages that help the participant maintain physical activity behaviors.
Other names: SMS, Short Message Service
The peer coach will deliver an intervention that will help participants maintain physical activity.
Other names: Peer Support, Peer Sustainability
Participants will be given written materials providing advice on maintaining their physical activity.
The Short Message System (SMS) intervention focuses on personalized, adaptive SMS messages that help the participant maintain physical activity behaviors. The peer coach will deliver an intervention that will help participants maintain physical activity.
Time frame: From Baseline to 15 Month Assessment
Participants will wear motion sensor on waist for 7 days
Time frame: At Baseline, 3 month assessment, 9 month assessment, and 15 month assessment.
Fatigue will be measured using the Fatigue Symptom Inventory (fatigue intensity and interference) scale.
Time frame: At Baseline, 3 month assessment, 9 month assessment, and 15 month assessment.
Self-perceived health will be measured using the EQ-5D questionnaire.
Time frame: At Baseline, 3 month assessment, 9 month assessment, and 15 month assessment.
Quality of life will be measured via the PROMIS Global Health questionnaire.
Time frame: At Baseline, 3 month assessment, 9 month assessment, and 15 month assessment.
Anxiety and depression will be measured using the Hospital Anxiety and Depression Scale.
Time frame: At Baseline, 3 months, 9 months, and 15 months
Stress will be measured using the Perceived Stress Scale
Time frame: At Baseline, 3 months, 9 months, 15 months
Social determinants of health will be measured using the Social Determinants of Health (SDoH) questionnaire.
Time frame: At Baseline, 3 months, 9 months, 15 months
Big five personality will be measured using a brief version of the Big Five Personality Inventory questionnaire.
Time frame: At Baseline, 3 months, 9 months, 15 months
Aerobic and resistance exercise will be measured using the Godin Aerobic Strength questionnaire.
Time frame: At Baseline, 3 months, 9 months, 15 months
Quality of life will be measured using the EQ-5D-5L questionnaire.
Time frame: At Baseline, 3 months, 9 months, 15 months
Social support for physical activity will be measured using the Social Support for PA questionnaire.
Time frame: Baseline, 3 months, 6 months, 9 months, 12 months, 15 months
Reflective, regulatory, and reflexive processes is being measured by the M-PAC physical activity questionnaire.
Time frame: At Baseline, 3 months, 9 months, 15 months
Barriers to exercise will be measured using the Perceived Barriers to Exercise questionnaire.
Contact information is provided by the study sponsor or research team.
Michelle Martin, PhD
CONTACT
Talia Williams, BA
CONTACT
University of Tennessee
Other
Making Healthy Habits Stick: Extended Contact Interventions to Promote Long-Term Physical Activity in Cancer Survivors
Acronym: HABITS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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