{"id":12,"date":"2018-02-23T12:13:45","date_gmt":"2018-02-23T12:13:45","guid":{"rendered":"https:\/\/websitedemos.net\/alex01\/?page_id=5"},"modified":"2023-07-05T12:59:20","modified_gmt":"2023-07-05T17:59:20","slug":"who-we-are","status":"publish","type":"page","link":"https:\/\/growingtreesinternational.org\/who-we-are","title":{"rendered":"WHO WE ARE"},"content":{"rendered":"\t\t
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WHO WE ARE<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\"\"<\/a><\/figure>

TAMARA D. OTEY PHD, RN<\/a><\/h4>

Assistant Professor<\/p><\/div><\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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BISHOP & MRS. VICTOR UZOSIKE<\/a><\/h4>

Presiding Bishop Kingdom Life Gospel Outreach Ministries International Inc. (KLGOMI)<\/p><\/div><\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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RHONDA NELSON<\/h4>

MPA, RN<\/p><\/div><\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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ANNETTE KINNARD<\/h4>

RDH<\/p><\/div><\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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\"\"<\/a><\/figure>

DR. LONNELL GANT<\/a><\/h4>

DNP<\/p><\/div><\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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Get Involved <\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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RESEARCH PARTICIPANTS BILL OF RIGHTS<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Growing Trees International Ministry requires that any person asked to take part as a subject in a research study will be asked to consent to such participation and they are entitled to receive the following list of rights written in a language in which the person is fluent. This list includes the right to:<\/p>

  1. Be informed of the nature and purpose of the study.<\/li>
  2. Be given an explanation of the procedures to be followed in the study, and any drug or device to be utilized.<\/li>
  3. Be given a description of any potential discomforts and risks reasonably to be expected from the study.<\/li>
  4. Be given an explanation of any benefits to the subject reasonably to be expected from the study, if applicable.<\/li>
  5. Be given a disclosure of any appropriate alternative procedures, drugs or devices that might be advantageous to the subject, and their relative risks and benefits.<\/li>
  6. Be informed of ongoing available medical support to subjects, if needed after the study, should complications arise related to the study.<\/li>
  7. Be given an opportunity to ask any questions concerning the study or the procedures involved.<\/li>
  8. Be instructed that consent to participate in the study may be withdrawn at any time and the subject may discontinue participation in the study without prejudice.<\/li>
  9. Be given a copy of the signed and dated written consent form if applicable.<\/li>
  10. Be given the opportunity to decide to consent or not to consent to a study without any element of force, fraud, deceit, duress, coercion, or undue influence on the subject\u2019s decision.<\/li><\/ol>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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    We welcome you to apply if you are:<\/strong><\/p>