Exercise + Self-Compassion Intervention for Depression

Sponsor
Western University, Canada (Other)
Overall Status
Recruiting
CT.gov ID
NCT04572035
Collaborator
(none)
60
1
3
20
3

Study Details

Study Description

Brief Summary

An alarming number of students report depressive symptoms that make it difficult to function academically. Previous research has indicated that exercise can be effective in treating mild-moderate depression. However, individuals with depression may struggle psychologically to adhere to exercise programs. Researchers have highlighted the potential role of self-compassion, a psychological approach that is useful in dealing with personal inadequacies, to facilitate health behaviour regulation. Behavioural coaching is another approach that consists of self-regulatory strategies such as action planning and less emphasis on emotion-focused strategies. The purpose of this study is to test the effectiveness of a structured exercise and psychoeducation program on improving depressive symptoms among inactive students with depression and to evaluate if the addition of psychological components (self-compassion or behavioural coaching) affects this effectiveness. Students with mild-to-moderate depression will refer themselves to participate or be referred/recommended by Student Health Services at Western University. The study will consist of attending 3 exercise + psychoeducation sessions per week for 10-weeks. Study participants will be randomly allocated to one of three groups; exercise only, exercise + self-compassion, or exercise + behavioral coaching. All will complete questionnaires before, after, and 3-months following the end of their sessions. It is expected that participants in the exercise + self-compassion or exercise + behaviour coaching groups will show greater improvements in their depressive symptoms, program adherence and follow-up exercise behaviour and depression after 3 months than the exercise only group and that the exercise + self-compassion group will be superior to the exercise + behavioural coaching group in those measurements.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behavioural Coaching
  • Behavioral: Self-compassion psychoeducation
  • Other: Exercise
N/A

Detailed Description

This is a 10-week randomized parallel study assessing the effectiveness of exercise in reducing depressive symptoms among students with mild-to-moderate depression. This study has three treatment arms: exercise; exercise + self-compassion; exercise + behavioral coaching. Each participant will be invited to attend 3 supervised group-based sessions each week either virtually through Zoom or in-person at the Exercise and Health Psychology Lab for 10 weeks. Senior undergraduate Kinesiology students will facilitate a personalized exercise program adapted to the participant's abilities, teach participants how to exercise, and gauge exercise intensity in a safe manner. The CANMAT guidelines will be implemented, with the program consisting of supervised moderate-intensity exercise sessions lasting 30-minutes (plus 10-minutes for warm-up and cool-down), 3 times weekly, for a period of 10-weeks. Participants will start exercising at a low intensity and progressively increase until they are consistently exercising at a moderate intensity. The exercise intervention will integrate moderate intensity aerobic and resistance training activities while accounting for the physical abilities and interests of the individual participant and theh group.The exercise + psychoeducation groups will receive equal contact supplemental individual manualized strategies each session (+15-20 minutes) centered either on behaviour change strategies (i.e., action planning, implementation intentions, relapse prevention, and goal setting) or self-compassion strategies (i.e., mindfulness, self-directed kindness meditations, and writing tasks). The manualized psychoeducation sessions will be group-based with the trainer that is supervising the exercise sessions. Participants will fill out surveys before, after and three months following the intervention period.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Feasibility, Acceptability and Effectiveness of a Structured Exercise + Psychoeducation Program for Students With Depression - A Proof of Concept Study
Actual Study Start Date :
Oct 1, 2020
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Exercise only

Undergraduate peer-facilitators part of a curricular kinesiology program will facilitate a personalized group-based exercise program adapted to the participant's abilities, teach participants how to exercise, and gauge exercise intensity in a safe manner (26). The CANMAT guidelines will be implemented, with the program consisting of supervised group-based moderate-intensity exercise sessions lasting 30-minutes (plus 10-minutes for warm-up and cool-down), 3 times weekly, for a period of 10-weeks. Participants will start exercising at a low intensity and progressively increase until they are consistently exercising at a moderate intensity. As a result of the uncertainty surrounding the pandemic, the intervention will be conducted either via a virtual platform or in-person at the Exercise and Health Psychology Lab, depending on the health and safety restrictions applicable to when the student enrolls and begins their program.

Other: Exercise
aerobic exercise program either delivered in a laboratory setting or via Zoom

Experimental: Exercise + Self-compassion

Participants will undergo the same exercise program as described in the exercise only treatment arm. Participants will receive equal contact supplemental individual manualized strategies each session (+15-20 minutes) centered on self-compassion strategies (i.e., mindfulness, self-directed kindness meditations, and writing tasks).

Behavioral: Self-compassion psychoeducation
self-compassion strategies (i.e., mindfulness, self-directed kindness meditations, and writing tasks)

Other: Exercise
aerobic exercise program either delivered in a laboratory setting or via Zoom

Experimental: Exercise + Behavioural Coaching

Participants will undergo the same exercise program as described in the exercise only treatment arm. Participants will receive equal contact supplemental individual manualized strategies each session (+15-20 minutes) centered on behaviour change strategies (i.e., action planning, implementation intentions, relapse prevention, and goal setting).

Behavioral: Behavioural Coaching
behaviour change strategies (i.e., action planning, implementation intentions, relapse prevention, and goal setting)

Other: Exercise
aerobic exercise program either delivered in a laboratory setting or via Zoom

Outcome Measures

Primary Outcome Measures

  1. Feasibility of intervention (recruitment) [From recruitment to baseline]

    Proportion of screened individuals choosing to participate (and reasons for not participating)

  2. Feasibility of intervention (compliance) [From baseline to 3-month follow-up]

    Proportion of program sessions attended (and reasons for non-attendance); proportion of participants that complete surveys

  3. Feasibility of intervention (completion) [From baseline to 3-month follow-up]

    Proportion of participants who drop-out prior to program completion

  4. Feasibility of intervention (delivery) [From recruitment to post-intervention]

    Proportion of eligible peer facilitators that maintain their participation in the full intervention

  5. Acceptability of intervention [Post-intervention]

    Treatment Acceptability Questionnaire - mean score ranging from 1 (low acceptability) to 7 (high acceptability)

  6. Effectiveness of intervention (depressive symptoms) [From baseline to 3-month follow-up.]

    Change in depressive symptoms measured by Patient Health Questionnaire 9 - total score ranges from 0 (no symptoms) to 27 (severe symptoms) for all treatment arms

  7. Effectiveness of intervention (exercise behaviour) [From baseline to 3-month follow-up.]

    Change in exercise measured by Leisure Time Exercise Questionnaire - calculate Leisure Score Index with higher values indicating higher exercise frequency/intensity for all treatment arms

Secondary Outcome Measures

  1. Effectiveness of psychological component (depressive symptoms) [From baseline to 3-month follow-up.]

    Treatment arm difference in changes in depressive symptoms measured by Patient Health Questionnaire 9 - total score ranges from 0 (no symptoms) to 27 (severe symptoms)

  2. Effectiveness of psychological component (exercise behaviour) [From baseline to 3-month follow-up.]

    Treatment arm difference in changes in exercise behaviour measured by Leisure Time Exercise Questionnaire - calculate Leisure Score Index with higher values indicating higher exercise frequency/intensity

  3. Effectiveness of psychological component (compliance) [From baseline to 3-month follow-up.]

    Treatment arm difference in compliance (attendance in program sessions)

Eligibility Criteria

Criteria

Ages Eligible for Study:
17 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Informed of the nature of the study and have agreed to and are able to read, review, and sign the informed consent form. The informed consent document will be written in English; therefore, the volunteer must have the ability to read and communicate in English.

  • Student participants 17 to 30 years of age, inclusive, at the time of screening.

  • Available and able to attend 3x group-based exercise training sessions per week.

  • Patient Health Questionnaire (PHQ)-9 score of >5

  • Godin Leisure-Time Exercise Questionnaire score of <14

  • Able to engage in physical activity as assessed by the PAR-Q

  • For Virtual Intervention Only: access to reliable internet connection and computer with a camera for the purpose of the Zoom Video calls

Exclusion criteria:
  • Participant receives pharmacological (i.e. medications listed in list of prohibited medications document) or psychotherapy treatment for depression or anxiety

  • Reports of suicide ideation (e.g., PHQ-9 item) and scores on the PHQ-9 >20 demonstrating severe depression

  • Failed safety screening for exercise without physician clearance

  • Participant initiates pharmacological or psychotherapy treatments for depression while in the study and/or participates in any other research that aims to target depression

Contacts and Locations

Locations

Site City State Country Postal Code
1 Western University London Ontario Canada N6A 3K7

Sponsors and Collaborators

  • Western University, Canada

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Eva Pila, Assistant Professor, Western University, Canada
ClinicalTrials.gov Identifier:
NCT04572035
Other Study ID Numbers:
  • 2020-0000-E
First Posted:
Oct 1, 2020
Last Update Posted:
Apr 27, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 27, 2022