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Clinical Trials/ACTRN12614000944639
ACTRN12614000944639
Terminated
未知

Effectiveness of a weight loss intervention based on diet and physical exercise to improve cognitive decision-making skills in adults with overweight and obesity compared with non-treated individuals.

School of Psychological Sciences - Monash University0 sites120 target enrollmentSeptember 3, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Overweight and obesity
Sponsor
School of Psychological Sciences - Monash University
Enrollment
120
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 3, 2014
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
School of Psychological Sciences - Monash University

Eligibility Criteria

Inclusion Criteria

  • Healthy weight adults: Age between 18 and 60; Body Mass Index (BMI) between 18 kg/m2 – 24\.9kg/m2
  • Excess weight adults: Age between 18 and 60; Body Mass Index (BMI) between 25 kg/m2 – 40kg/m2

Exclusion Criteria

  • Overweight participants who are taking part in the weight management program: (1\) current or previous pregnancy (within past 6 months) or lactating; (2\) history of substance
  • use (drug or alcohol); (3\) history of head trauma or neurological illness impacting Central Nervous System or undergone radiation treatment; (4\) current diagnosis of depression; (5\) unable to read and converse in English; (6\) clinically diagnosed or screen positive for disordered eating.
  • Normal\-weight and overweight participants no taking part in the weight management program: (1\) current or previous pregnancy (within past 6 months) or lactating; (2\) current or recent history of health condition (including cancer; thyroid disease; surgery; hepatic disease; stage 3\-5
  • CKD; eating disorders; those who have previously undergone radiation treatment); (3\) current comorbid medical conditions associated with excess weight (e.g., type II diabetes, hypertension); (4\) has undergone weight loss surgery; (5\) taking weight loss drugs; (6\) history of substance use (drug or alcohol); (7\) history of head trauma or neurological illness impacting Central Nervous System; (8\) current diagnosis of depression; (9\) has lactose intolerance; (10\) unable to read and converse and English; (11\) clinically diagnosed or screen positive for disordered eating using.
  • Eligible overweight and obese participants are healthy volunteers. Participants will be asked to provide a finger prick blood sample in order to measure fasting plasma glucose. If a blood glucose reading greater than or equal to 7\.0mmol/l is recorded which is indicative of diabetes, the participant will be referred to their GP and not able to proceed further with the study. Furthermore, blood pressure will be measured with an automated sphygmomanometer. If a blood pressure reading greater than or equal to 140/90 mm Hg is recorded which is indicative of hypertension, the participant will not be able to proceed further with the study.

Outcomes

Primary Outcomes

Not specified

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