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OpenTrials
Completed

NCT Number: NCT05997251

The Relationship of DASH and Mediterranean Diet Score With Serum Adiponectin Levels in Patients With Spinal Cord Injury

The aim of this study is to reveal the relationship of DASH and Mediterranean diet score with anthropometric measurements and serum adiponectin level in individuals with spinal cord injury. This research was planned as a cross-sectional, case-control study. With the data to be obtained from the research, information will be obtained about the hormonal or biochemical basis of metabolic disorders such as atherosclerosis and insulin resistance that may occur in individuals with spinal cord injury in the long term.

20 individuals with Spinal Cord Injury will be included in the study, and the results of the patients will be compared with 20 healthy individuals. In order to determine the food consumption status of the patients, a 1-day food consumption record will be requested. DASH diet score and Mediterranean diet score will be calculated from dietary records. After 8 hours of fasting, 3 ml of peripheral blood will be taken for the measurement of adiponectin between 08:00 and 09:00 in the morning from the individuals in the study and control groups. Adiponectin level will be measured and its correlation with DASH diet score and Mediterranean diet score will be examined.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Ankara Bilkent City Hospital Physical Treatment and Rehabilitation Hospital

Ankara, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inclusion criteria (Study group)
  • Having spent at least 6 months after spinal cord injury
  • 1st motor neuron injury
  • Being between the ages of 18-65
  • Giving consent to participate in the study Inclusion criteria (Control group)
  • Being between the ages of 18-65
  • Giving consent to participate in the study

Exclusion criteria

  • Exclusion criteria (Study group)
  • Having an additional disease to the spinal cord injury
  • Having a 2nd motor neuron lesion

Exclusion criteria

(Control group)

  • Having any disease

Treatment and study plan

Keeping a 1-day food consumption record by the patient

Other

Checking and receiving the 1-day food consumption record recorded by the patient by the researcher

Measurement of adiponectin level

Other

Adiponectin level will be measured for each group

Primary outcomes

  1. Adiponectin level

    Time frame: Will be measured at inclusion

    Adiponectin level will be measured from peripheral blood

  2. DASH diet score

    Time frame: Will be measured at inclusion from one day dietary record

    Will be measured at inclusion from one day dietary record

  3. Mediterrenian diet score

    Time frame: Will be measured at inclusion from one day dietary record

    Will be measured at inclusion from one day dietary record

Secondary outcomes

  1. Whole blood count

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

  2. Fasting blood glucose

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

  3. Total cholesterol

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

  4. LDL

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

  5. HDL

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

  6. TG

    Time frame: Will be measured at inclusion

    Will be measured at inclusion

Sponsors and collaborators

Lead sponsor

Ankara City Hospital Bilkent

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Aug 18, 2023
Registry last updated
Aug 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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