ACTRN12622001261707
Completed
未知
A Comparison of Goal-Oriented, Guided Imagery versus SMART Goal Setting Interventions on Physical Activity Levels in Young, Inactive Adults with Overweight or Obesity: A Randomised Controlled Trial Pilot Study
Swinburne university0 sites60 target enrollmentSeptember 21, 2022
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- overweight
- Sponsor
- Swinburne university
- Enrollment
- 60
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Participants eligible for the trial must comply with all the following criteria at randomisation:
- •men between the ages of 18 and 34 years;
- •overweight or obese but classified within only the following four Body Mass Index (BMI) categories: (a) Overweight – BMI greater than or equal to 25 to 29\.9 kg/m^2; (b) Obesity – BMI greater than or equal to 30 kg/m^2; (c) Obesity class I – BMI 30 to 34\.9 kg/m^2; or (d) Obesity class II – BMI 35 to 39\.9 kg/m^2\.
- •individuals who fall under ‘low/moderately active’ in the physical activity category of the International Physical Activity Questionnaire;
- •Male participants will be excluded if their waist circumference is less than 99 or greater than 125\. Female participants will be excluded if their waist circumference is less than 80 or greater than 110\.
- •Adults residing in Australia;
- •no mobility impairment;
- •free for at least six months of musculoskeletal injury requiring medical or allied health intervention or treatment; and
- •free of ongoing use of pain medication for more than two episodes of one week, based on advice from allied health professional.
Exclusion Criteria
- •Participants will be excluded based on the following
- •Obesity category class III includes morbidly obese individuals who are associated with very high risk of comorbidities, hence this class is excluded to ensure protection of individuals from potential harm.
- •In addition:
- •6\) Participants will be excluded based on mobility impairment.
- •7\) Participants will be excluded if they are not at least 6 months free of musculoskeletal injury requiring medical or allied health intervention or treatment; and free of ongoing use of pain medication for more than 2 episodes of one week as suggested by an allied health professional
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Phase 2
Comparison between the effects of guided imagery and progressive muscle relaxation on quality of lifeIRCT2016072512257N5Vice chancellor for Research, Zanjan University of Medical Sciences64
Completed
Not Applicable
The Effect of Guided imagery on Anxiety and Quality of sleep of Hemodialysis PatientsIRCT2016120931312N1Vice chancellor for research, Kashan University of Medical Sciences70
Completed
Not Applicable
Comparing the effect of GUIDED IMAGERY and CRYOTHERAPY(cold compress) on post operative pain severity and vital signs among laparoscopic cholecystectomy inpatients in Teaching Hospitalsaparoscopic cholecystectomy.Calculus of gallbladder with acute cholecystitis with obstructionK80.01IRCT20230723058896N1Oroumia University of Medical Sciences93
Completed
Not Applicable
Effect of guided imagery on stigma and emotion regulation in hemodialysis patientsIRCT20151107024919N17Kerman University of Medical Sciences56
Recruiting
Not Applicable
Evaluation of the effectiveness of Guided Imagery on anxiety and breast milk volume of mothers of preterm infantsIRCT20210324050763N1Mashhad University of Medical Sciences60