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A Virtual Reality Exposure Intervention on Social Physical Anxiety in Women With Obesity (SPA-VR)

Primary Purpose

Obesity, Exercise, Virtual Reality

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exposure intervention in virtual reality
Exercise
Placebo
Sponsored by
Universite du Quebec en Outaouais
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • woman
  • inactive (<150 min. of moderate to vigorous PA / week )
  • aged between 18 and 45 years
  • BMI ≥ 30 kg / m2
  • to be able to go to Université du Québec en Outaouais twice a week

Exclusion Criteria:

  • to have a low to moderate social physical anxiety level (SPA score <27/45 on the physical and social anxiety scale )
  • suffer from hypersensitivity to motion sickness
  • to be pregnant or plan to become over the next year
  • to take medication that may influence weight
  • to have undergone bariatric surgery
  • to have a contraindication to physical activity
  • to have participated in a physical activity program in the last 6 months supervised
  • to have an intellectual disability, and have a severe and persistent psychiatric problem (psychosis, bipolar disorder).

Sites / Locations

  • UQORecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Virtual reality and exercice

Placebo and exercice

waiting list

Arm Description

This group will receive the exposure intervention in virtual reality and physical activity during 12 weeks

This group will receive the placebo intervention (relaxation) and physical activity during 12 weeks

This group will receive no intervention during 12 weeks, then will be randomized in the experimental or placebo group

Outcomes

Primary Outcome Measures

Feasibility of the protocol and the intervention
The feasibility of the protocol will be assessed at the end of the study using the following criteria: i) the recruitment rate (number of participants recruited per month), ii) the retention rate (number of participants who have completed all the assessments and focus group and reason for dropout), iii) percentage of missing data (number of missing data out of number of total data) and iv) acceptance of randomization. The feasibility of the intervention will be evaluated at the end of the study using the following criteria: v) the participation rate (number of eligible participants who agreed to participate in the study), vi) the participation rate adherence (number of participants who completed the 8 psychological intervention sessions), vii) the attrition rate (number of participants who abandoned the psychological intervention and reasons). The achievement of the following criteria will be considered as a success factor in terms of feasibility (14, 23): i) recruitment rate ≤ 5.6,
Acceptability of the protocol and the intervention
The acceptability of the protocol and the intervention will be qualitatively assessed through 5 to 7 semi-structured discussion groups by teleconference via the zoom platform. The participants will be interviewed for 75 minutes in sub-groups of 6 to 8 participants on their perception, opinion and experience regarding the intervention and the implementation of the protocol (barriers, facilitators, satisfaction, perceived benefits, recommendation and improvement). An interview guide constructed for the purpose of the study will ensure consistency of the themes explored between the different groups while guiding the group facilitation.

Secondary Outcome Measures

Social physical anxiety change (0-12 weeks)
Social physical anxiety scale (validated questionnaire)
Adherence to the physical activity (PA) intervention
Adherence to the PA intervention will be calculated as a percentage from the total number of sessions performed out of the 36 prescribed sessions (frequency).
Compliance with the PA intervention
Compliance with the PA intervention will be calculated as a percentage from the number of sessions for which the participant will have prescribed the prescription compared to all sessions. For these calculations, data from heart rate monitors worn by participants during PA sessions and diaries completed by participants and the kinesiologist will be used.
Physical activity change (0-12 weeks)
Triaxial accelerometer (Actigraph® wGT3X-BT) worn on the hip for 7 days
Persistance in the practice of PA after the intervention
Triaxial accelerometer (Actigraph® wGT3X-BT) worn on the hip for 7 days

Full Information

First Posted
November 3, 2020
Last Updated
October 31, 2022
Sponsor
Universite du Quebec en Outaouais
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1. Study Identification

Unique Protocol Identification Number
NCT04630184
Brief Title
A Virtual Reality Exposure Intervention on Social Physical Anxiety in Women With Obesity
Acronym
SPA-VR
Official Title
Development and Impact of a Virtual Reality Exposure Intervention on Social Physical Anxiety During Physical Activity in Women With Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
March 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universite du Quebec en Outaouais

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objectives of the project are to: i) assess the feasibility and acceptability of the protocol and the VR exposure intervention in women with obesity, and ii) obtain an estimate of the effect of VR exposure intervention associated with an exercise training on SPA, compliance, adherence and persistence to the exercise training, as well as persistence in PA practice in the middle term to calculate the sample size for a future larger randomized controlled trial (RCT) in women with obesity. A RCT of feasibility will be carried out. Forty-five women with obesity and a high level of SPA will be randomized into one of the following three groups: 1) Exercice and VR exposure (Ex + expo), 2) Exercise and psychological intervention control (Ex + control) or 3) waiting list (WL). The interventions will have a physical exercise training (identical for all) and a psychology intervention (different according to the condition: VR exposure or control). The feasibility and acceptability of the protocol and the VR exposure intervention will be assessed at the end of the study. SPA, PA practice, anthropometry, internalization of weight bias, body appreciation, perceived pleasure, motivational regulation, self-efficacy, affects as well as perception effort will be evaluated with questionnaires and scales validated before and after the intervention and 6 months after the end of the intervention. Sociodemographic data, depressive symptoms, problematic eating behaviors and propensity to immersion will be assessed during the initial visit only. Adherence, adherence and persistence to the PA program will be calculated at the end of the intervention. Persistence in PA practice will be calculated using data collected immediately after the end of the intervention and 6 months after the intervention.
Detailed Description
Several studies show that a high level of social physical anxiety (SPA) can lead to avoidance and poor adherence to physical activity (PA) programs. Although this link is known and a high level of SPA is frequently found in women with obesity, no psychological intervention specific to the treatment of SPA has been developed to date. Exposure therapy is the treatment of choice for general social anxiety. However, this format of therapy can cause great discomfort for the patient and prevents complete control of the environment by the clinician. Virtual reality (VR), commonly employed in the treatment of anxiety disorders, offers a solution to these problems by allowing exposure to human stimuli in an adaptable environment and under the control of the clinician, with a reduction in stress patient discomfort. The objectives of the project are to: i) assess the feasibility and acceptability of the protocol and the VR exposure intervention in women with obesity, and ii) obtain an estimate of the effect of VR exposure intervention associated with an exercise training on SPA, compliance, adherence and persistence to the exercise training, as well as persistence in PA practice in the middle term to calculate the sample size for a future larger randomized controlled trial (RCT) in women with obesity. A RCT of feasibility will be carried out. Forty-five women with obesity and a high level of SPA will be randomized into one of the following three groups: 1) Exercice and VR exposure (Ex + expo), 2) Exercise and psychological intervention control (Ex + control) or 3) waiting list (WL). The interventions will have a physical exercise training (identical for all) and a psychology intervention (different according to the condition: VR exposure or control). The feasibility and acceptability of the protocol and the VR exposure intervention will be assessed at the end of the study. SPA, PA practice, anthropometry, internalization of weight bias, body appreciation, perceived pleasure, motivational regulation, self-efficacy, affects as well as perception effort will be evaluated with questionnaires and scales validated before and after the intervention and 6 months after the end of the intervention. Sociodemographic data, depressive symptoms, problematic eating behaviors and propensity to immersion will be assessed during the initial visit only. Adherence, adherence and persistence to the PA program will be calculated at the end of the intervention. Persistence in PA practice will be calculated using data collected immediately after the end of the intervention and 6 months after the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Exercise, Virtual Reality

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Masking Description
The reserarch assistant (for assesement) will be blind of the group allocation, as well as the kinesiologist (but not the psychologist).
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual reality and exercice
Arm Type
Experimental
Arm Description
This group will receive the exposure intervention in virtual reality and physical activity during 12 weeks
Arm Title
Placebo and exercice
Arm Type
Placebo Comparator
Arm Description
This group will receive the placebo intervention (relaxation) and physical activity during 12 weeks
Arm Title
waiting list
Arm Type
No Intervention
Arm Description
This group will receive no intervention during 12 weeks, then will be randomized in the experimental or placebo group
Intervention Type
Behavioral
Intervention Name(s)
Exposure intervention in virtual reality
Intervention Description
6 sessions of 45 minutes weekly and 2 follow-up meetings (3 and 6 weeks after the weekly follow-up) with cognitive restructuring and VR exposure supervised by psychologists
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Participants will have to go twice a week, for 12 weeks to carry out 2 individual endurance training sessions of 45 minutes (moderate to vigorous intensity), supervised by a kinesiologist. Participants will also have to complete a 3rd 60-minute endurance session at home (or two 30-minute sessions).
Intervention Type
Behavioral
Intervention Name(s)
Placebo
Intervention Description
6 sessions of 45 minutes weekly and 2 follow-up meetings (3 and 6 weeks after the weekly follow-up) Discussion around social physical anxiety, stress management (relaxation and breathing) supervised by psychologists
Primary Outcome Measure Information:
Title
Feasibility of the protocol and the intervention
Description
The feasibility of the protocol will be assessed at the end of the study using the following criteria: i) the recruitment rate (number of participants recruited per month), ii) the retention rate (number of participants who have completed all the assessments and focus group and reason for dropout), iii) percentage of missing data (number of missing data out of number of total data) and iv) acceptance of randomization. The feasibility of the intervention will be evaluated at the end of the study using the following criteria: v) the participation rate (number of eligible participants who agreed to participate in the study), vi) the participation rate adherence (number of participants who completed the 8 psychological intervention sessions), vii) the attrition rate (number of participants who abandoned the psychological intervention and reasons). The achievement of the following criteria will be considered as a success factor in terms of feasibility (14, 23): i) recruitment rate ≤ 5.6,
Time Frame
At the end of the study (+ 36 weeks)
Title
Acceptability of the protocol and the intervention
Description
The acceptability of the protocol and the intervention will be qualitatively assessed through 5 to 7 semi-structured discussion groups by teleconference via the zoom platform. The participants will be interviewed for 75 minutes in sub-groups of 6 to 8 participants on their perception, opinion and experience regarding the intervention and the implementation of the protocol (barriers, facilitators, satisfaction, perceived benefits, recommendation and improvement). An interview guide constructed for the purpose of the study will ensure consistency of the themes explored between the different groups while guiding the group facilitation.
Time Frame
At the end of the intervention (+ 12 weeks)
Secondary Outcome Measure Information:
Title
Social physical anxiety change (0-12 weeks)
Description
Social physical anxiety scale (validated questionnaire)
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Adherence to the physical activity (PA) intervention
Description
Adherence to the PA intervention will be calculated as a percentage from the total number of sessions performed out of the 36 prescribed sessions (frequency).
Time Frame
At the end of the PA intervention (after 12 weeks)
Title
Compliance with the PA intervention
Description
Compliance with the PA intervention will be calculated as a percentage from the number of sessions for which the participant will have prescribed the prescription compared to all sessions. For these calculations, data from heart rate monitors worn by participants during PA sessions and diaries completed by participants and the kinesiologist will be used.
Time Frame
At the end of the PA intervention (after 12 weeks)
Title
Physical activity change (0-12 weeks)
Description
Triaxial accelerometer (Actigraph® wGT3X-BT) worn on the hip for 7 days
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Persistance in the practice of PA after the intervention
Description
Triaxial accelerometer (Actigraph® wGT3X-BT) worn on the hip for 7 days
Time Frame
Immediately after the intervention and at the end of the study (after 12 weeks and 36 weeks)
Other Pre-specified Outcome Measures:
Title
Propensity to immersion
Description
Validated questionnaire
Time Frame
Before the intervention (baseline)
Title
The feeling of presence in immersion the feeling of presence in immersion
Description
Gatineau presence questionnaire
Time Frame
after each virtual reality session (weeks 1, 2, 3, 4, 5,6 , 9 amd 12)
Title
Cybermalaise
Description
Simulator Sickness Questionnaire
Time Frame
before and after each virtual reality session (weeks 1, 2, 3, 4, 5,6 , 9 amd 12)
Title
Sociodemographic data
Description
age, sex,ethnocultural group, level of education, professional status
Time Frame
before the intervention (baseline)
Title
Depressive symptoms
Description
Center Epidémiologic Scale-Depression-French ; scale (0-3) score range (0-60) higher score = higher depressive symptoms
Time Frame
before the intervention (baseline)
Title
Food disorder
Description
Eating Attitudes Test-26 ; scale (0-3) score range (0-78), Higher scores indicating greater risk of an eating disorder
Time Frame
before the intervention (baseline)
Title
Weight Bias Internalisation change (0-12 weeks)
Description
Modified Weight Bias Internalisation Scale, scale (1-7), range score (11-77), higher score = higher Weight Bias Internalization)
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Body composition change (0-12 weeks)
Description
bio-impedance balance (Tanita MC 780U) made by research assistant
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Body index mass change (0-12 weeks)
Description
scale and measuring rod to measure the size made by research assistant
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Waist circumference change (0-12 weeks)
Description
tape measure made by research assistant
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Body Appreciation change (0-12 weeks)
Description
Body Appreciation Scale-2, scale (1-5) score range (1-5), higher score = higher body satisfaction
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Perceived pleasure in physical activity in general (0-12 weeks)
Description
Physical Activity Enjoyment Scale, scale (1-7) score (1-7) higher score = higher enjoyment
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Motivation change (0-12 weeks)
Description
Behavioural Regulation In Exercise Questionnaire, scale (0-4), Higher, positive scores indicate greater relative autonomy; lower, negative scores indicate more controlled regulation.
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Affects during exercise change (0-12 weeks)
Description
Felt Arousal Scale (score 1-6) higher score = higher felt arousal + Feeling Scale (score -5,5) higher score higher pleasure
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Self-efficacy change (0-12 weeks)
Description
Self efficacy scale (Bandura), scale (0-100) score range (0-100) higher score = higher self efficacy
Time Frame
Before and after intervention (Baseline and after 12 weeks)
Title
Perception effort change (0-12 weeks)
Description
Borg scale, scale and score range (0-10), higher score = higher perception of effort
Time Frame
Before and after intervention (Baseline and after 12 weeks)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: woman inactive (<150 min. of moderate to vigorous PA / week ) aged between 18 and 45 years BMI ≥ 30 kg / m2 to be able to go to Université du Québec en Outaouais twice a week Exclusion Criteria: to have a low to moderate social physical anxiety level (SPA score <27/45 on the physical and social anxiety scale ) suffer from hypersensitivity to motion sickness to be pregnant or plan to become over the next year to take medication that may influence weight to have undergone bariatric surgery to have a contraindication to physical activity to have participated in a physical activity program in the last 6 months supervised to have an intellectual disability, and have a severe and persistent psychiatric problem (psychosis, bipolar disorder).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
aurelie Baillot
Phone
8199437561
Email
aurelie.baillot@uqo.ca
Facility Information:
Facility Name
UQO
City
Gatineau
State/Province
Quebec
ZIP/Postal Code
J8X 3X7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
aurelie baillot, phD
Phone
(819) 595-3900
Ext
1995
Email
aurelie.baillot@uqo.ca

12. IPD Sharing Statement

Learn more about this trial

A Virtual Reality Exposure Intervention on Social Physical Anxiety in Women With Obesity

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