The Supporting Her In Navigating Exercise Program: Examining Peer Support to Promote Exercise Among Undergraduate Women

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorLakehead University

About this trial

The purpose of this randomized controlled pilot trial is to test the effectiveness of a six-week tailored physical activity program with and without peer mentoring on the psychological constructs and exercise behaviour of inactive undergraduate women. The objectives are to:

* Quantify the degree to which a peer-mentorship intervention affects exercise motivation determined through three basic psychological needs (i.e., autonomy, competence, and relatedness). * Examine general psychological distress and exercise engagement throughout the study. * Qualitatively explore participants' experiences following the completion of the program using an open-ended survey to gain a better understanding of its impact.

Researchers will compare the parallel arm conditions to see how the inclusion of social support impacts exercise engagement.

Participants will be asked to engage in exercise three times a week at the campus gym; those in the intervention condition will have an assigned peer-mentor who will join them for one weekly session and virtually communicate with them between sessions.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Identify as a woman

Full-time undergraduate student at Lakehead University

Classified as an exercise initiate (e.g., report one or fewer bouts of exercise per week)

Reported an absence of health risks that would interfere with exercise engagement as determined by the Get Active Questionnaire

Disqualifiers

Identify as a man

Not enrolled as a full-time undergraduate student at Lakehead University

Report the presence of health risks that would interfere with exercise engagement

Meet the national physical activity guidelines (e.g., 150 minutes of moderate to vigorous exercise per week)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intervention

    Other intervention

    Participants will be encouraged to engage in independent exercise twice a week for 30 minutes. They will be randomly assigned to a peer-mentor, with whom they will engage in on-on-one exercise once a week for 30 minutes. Between sessions, they will engage in virtual communication with each other for about 30 minutes each week. Each participant-mentor duo will continue this protocol for 6-weeks.

  • Control

    Other intervention

    Participants will be encouraged to engage in exercise three times a week for thirty minutes, over a span of 6-weeks.

Treatment groups

24 Participants
are divided into 2 treatment groups
Group A: Exercise plus mentorExperimental treatment 1 intervention
Group B: Exercise aloneActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Psychological Needs Satisfaction in Exercsie Scale

Participants' exercise motivation, focused on the psychological needs and specific regulations, will be assessed quantitatively using The Psychological Needs Satisfaction in Exercise Scale. This 18-question tool, participants will evaluate each statement based on how it applied to them over the past week on a six-point scale (1= false, 6= true). In this scale, six statements are allotted for each of the three basic needs (e.g., autonomy, competence, and relatedness) in the context of exercise engagement. Subscale scores will be calculated by averaging the six items assigned to each basic psychological need, with higher scores being more indicative of greater self-determination and lower of less.

Time frame
During enrollment at baseline, after week 3, and at the end of the study at week 6
2

Behavioural Regulation in Exercise Questionnaire- 3

This questionnaire will be used to to gauge where an individual falls on the six-point motivational continuum, as it relates to exercise engagement. This will be assessed quantitatively using the Behavioural Regulation in Exercise Questionnaire-3, as participants will evaluate each statement based on how it applied to them over the past week. The 24-questions in this measure operate on a five-point Likert scale (0= not true for me, 2= sometimes true for me, 4= very true for me). In this questionnaire, four statements have been allocated for each of the six types of regulation/motivation (e.g., motivation, introjected regulation, identified regulation, integrated regulation, intrinsic regulation, external regulation). Subscale scores will be calculated by averaging the six items assigned to each basic psychological need, with higher scores being more indicative of greater intrinsic motivation and lower of greater extrinsic motivation.

Time frame
During enrollment at baseline, after week 3, and at the end of the study at week 6

Secondary outcomes

1

Depression Anxiety Stress Scale- Short Form

Participants' general psychological distress will be quantitatively measured through the Depression Anxiety Stress Scale- Short Form. The 21-question scale operates on a four-point Likert scale (0= never, 1= sometimes, 2= often, 3= almost always), and asks participants to evaluate each statement based on how it applied to them over the past week. In this scale, seven questions were allotted to each of the three categories (e.g., depression, anxiety, and stress). When scoring the DASS-21, the scores for each of the three categories are independently summed to gain a final score, with higher scores being indicative of severe psychological distress and lower scores suggest average or typical symptoms.

Time frame
During enrollment at baseline, following week 3, and at the end of the study at week 6
2

Exercise Tracking- Gym location

Participants' exercise engagement will be measured via a virtual exercise monitoring platform, Strava. Participants will upload their workouts each week, revealing the area of the gym they used (e.g., Hangar, Wolf Den, Basement).

Time frame
From enrollment to the end of the program at 6 weeks
3

Exercise Tracking- Duration

Participants' exercise engagement will be measured via a virtual exercise monitoring platform, Strava. Participants will upload their workouts each week, revealing the duration of their session.

Time frame
From enrollment to the end of the program at 6 weeks
4

Exercise Tracking- Workout Details

Participants' exercise engagement will be measured via a virtual exercise monitoring platform, Strava. Participants will upload their workouts each week, revealing the type of workout they engaged in (e.g., cardio, upper body strength, lower body strength, full body strength training).

Time frame
From enrollment to the end of the program at 6 weeks

Other outcomes

1

Qualitative Experiential Accounts- Open Ended Questionnaire

Upon completion of the program, all participants will complete an open-ended questionnaire to gain an in-depth understanding of their program experiences. This questionnaire is comprised of open-ended questions adopted from previous research in this area and includes questions regarding topics such as exercise habits, motivation, three basic psychological needs, and perceptions of the SHINE program.

Time frame
Findings will be collected upon completion of the program, at the end of week 6.
2

Facility Usage Data- Frequency

Facility usage data will be monitored through Lakehead University's Athletics platform and will include dates and times signed in at the gym.

Time frame
From enrollment to the end of the program at 6 weeks
3

Communication Data- Frequency

Communication usage data between participants and their peer mentors will be monitored by the student researcher through GroupMe, an online messaging platform.

Time frame
From enrollment to the end of the program at 6 weeks
4

Demographic Information- Program of study

Demographic questions to assist the researchers in understanding the population characteristics will be asked at the outset of the study, including their program of study.

Time frame
During enrollment at baseline

Sponsors and contacts

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Lakehead University

Lead sponsor

Canadian Institutes of Health Research (CIHR)

Collaborator

St. Joseph's Care Group

Collaborator