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Effect of Cognitive Behavioral Therapy and Phototherapy on Glycosylated Hemoglobin, CLOCK Genes and Quality of Life in Patients With Type 2 Diabetes Mellitus and Insomnia

C

Centro Interdisciplinario de Ciencias de la Salud Unidad Santo Tomás

Status

Completed

Conditions

Type 2 Diabetes

Treatments

Behavioral: Effect of Cognitive Behavioral Therapy with Phototherapy in glycated hemoglobin, CLOCK genes and quality of life in patients with type 2 diabetes mellitus and insomnia

Study type

Interventional

Funder types

Other

Identifiers

NCT06264661
HJM 006/22-R

Details and patient eligibility

About

Purpose: To analyze the efficiency of Cognitive Behavioral Intervention in combination with phototherapy to reduce insomnia and improve glycemic control, quality of life, and CLOCK genes expression in patients with type 2 diabetes mellitus. Methods: Clinical, quasi-experimental, pre-post, explanatory, non-probability sampling. Subjects were invited to participate in Hospital Juárez de México. They received eight sessions of Cognitive Behavioral Therapy in combination with phototherapy. The assessment was carried out with validated instruments for Mexican population and gene expression was evaluated by real-time PCR.

Enrollment

23 patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Have a medical record in the Endocrinology service at the Hospital Juarez de Mexico

  • Patients with type 2 diabetes mellitus
  • Age between 40 and 60 years
  • Present Insomnia based on the criteria of The Diagnostic and Diagnostic Manual Statistics of Mental Disorders (DSM-V) which defines insomnia such as predominant dissatisfaction with the quantity or quality of sleep, associated with one (or more) of the following symptoms: a) Difficulty starting the dream,or b) Difficulty maintaining sleep, characterized by awakenings frequent and c) Waking up early in the morning with inability to return to sleep; with clinically significant distress or social impairment, work, educational, academic, behavioral or other important areas of operation, at least three nights a week, for a minimum of three months even with favorable sleeping conditions.
  • Sign an informed consent letter and agree to participate in the study.
  • Accept taking a blood sample pre and post intervention
  • HbA1c level above 6.1% (120 mg/dL;7 mmol/L) or BMI less than 34.9 units

Exclusion criteria

  • Do not agree to sign the informed consent
  • Have a previous psychiatric diagnosis
  • Have neurological disorders
  • Be diagnosed with type 1 diabetes mellitus or BMI greater than 35 units
  • Missing more than 20% of the sessions (2 sessions)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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