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IRCT20190809044485N1 IRCT 2019-09-28 College of Nursing, University of Baghdad Targeting Eating Triggers: A Tailored Nurse-led Intervention for Body Weight Control Targeting Eating Triggers Trial (TETT) Influence of A Tailored Nurse-Led Intervention on Controlling Body Weight among Clients Who are Medically Diagnosed with Obesity 2019-09-27 anticipated 128 Complete https://irct.ir/trial/41412 interventional Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: In order to maintain a transparent and scientific-based randomization process, simple randomization will be used in assigning participants (individuals: persons who are medically diagnosed with obesity), to treatment and control groups, assuming that each participant has an equal chance of being assigned to any group. The simple randomization procedure would involve throwing a dice (eg, below and equal to 3  =  control, over 3  =  treatment). No allocation concealment will be carried out. N/A Overweight & Obesity. Intervention 1: Intervention group: The starting point of the interventional phase will start by asking the subjects to respond to “What Triggers Your Eating? Questionnaire” (Nash, 1997). This mandatory step will help in categorizing the subjects according to their dominant eating trigger. Interventional group subjects in the intervention group will be armed with orally and in a written form simple, yet specific instructions to enable them managing their dominant eating trigger. The experimental group will be contacted after 30 days to see the influence of following the given instruction on the subject’s body weight. Intervention 2: Control group: It is planned that 64 subjects will be requited to be in this group. After determining their eating behavior dominant trigger, no instructions will be given to the subjects in the control group during the study course. Yes - There is a plan to make this available What will be shared: The researcher is acknowledging the scientific community to have verifiable findings of the study. sharing plan includes making all the related data available through publishing the study report in peer-reviewed reputable journals. When: God willing, once finishing the process of data collection, analysis and successfully publishing the manuscript, all the related files will become available for 6 months after publications To whom: All the related files will be shared with any scientific interested parties. Conditions: It may be used after seeking the author's permission and acknowledging his contribution. Where to obtain: The author's professional e-mail that will be available with the published manuscript can be used to contact the author. e-Mail: s.al-fayyadh@conursing.uobaghdad.edu.iq How to obtain: N/A Comments: Profound appreciations are due to the IRCT members for their genuine efforts in helping researchers fulfiling their academic endeavours.
public Sadeq AL-Fayyadh
Al Karkh,Ajnadine neighborhood, House No 3, Street No 62, Section No 863
Baghdad Iraq 10001 +964 1 521 1494 s.al-fayyadh@conursing.uobaghdad.edu.iq The University of Baghdad, College of Nursing scientific Sadeq AL-Fayyadh
Baghdad, Al Karkh,Ajnadine neighborhood
Baghdad Iraq 10001 +964 1 521 1494 s.al-fayyadh@conursing.uobaghdad.edu.iq University of Baghdad, College of Nursing Iraq Consent and compliance with all aspects of the study protocol, methods, providing data during follow-up contact Male & female patients, who are 18-70 years old at the time of data collection phase Voluntarily seeking professional help from Obesity Control Centers in Baghdad City 18 years 70 years Both Involvement with any other ongoing studies. Medically diagnosed with psychotic diseases Morbidly ill subjects, whereas their physical & mental capacity are impaired E66.0 Obesity due to excess calories Lifestyle N/A Intervention group: The starting point of the interventional phase will start by asking the subjects to respond to “What Triggers Your Eating? Questionnaire” (Nash, 1997). This mandatory step will help in categorizing the subjects according to their dominant eating trigger. Interventional group subjects in the intervention group will be armed with orally and in a written form simple, yet specific instructions to enable them managing their dominant eating trigger. The experimental group will be contacted after 30 days to see the influence of following the given instruction on the subject’s body weight. Control group: It is planned that 64 subjects will be requited to be in this group. After determining their eating behavior dominant trigger, no instructions will be given to the subjects in the control group during the study course. Body weight in Kg. Timepoint: The body weight will be initially measured at the first meeting with the target subject before offering the educational intervention. After four weeks of the first meeting, the body weight will be re-checked to examine the effectiveness of the intervention on the body weight. Method of measurement: Self-report of body weight reduction in Kg by calculating the Body Mass Index. The author of the trial is the funding source Approved 2017-12-03 Research Ethical Approval Committee, at the College of Nursing Bab AL-Muadum, Baghdad Baghdad Iraq