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NCT07226128Toboroz

The Effects of Cognitive Behavioral Therapy on Insulin Resistance in People With HIV

A Randomized, Controlled Trial Assessing the Effects of Cognitive Behavioral Therapy to Prevent Worsening Insulin Resistance in Depressed, Virologically-Suppressed, Antiretroviral-Treated Adults With HIV

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. aug. 21.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

The goal of this clinical trial is to learn if depression treatment improves insulin resistance, or how the body uses insulin to lower blood sugar, in people with HIV on HIV treatment. Researchers will compare an internet-based (online) depression treatment program called cognitive behavioral therapy with depression education. In the online group, participants will undergo 9 weekly treatment sessions. The education group will receive learning materials about depression and will be monitored every month. All participants will have 4 study visits over 12 months.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
150 (tervezett)
Első benyújtás
2025. nov. 5.
Kezdés
2026. ápr. 10.
Elsődleges befejezés
2029. aug. 31.
Fő szponzor
Indiana University
Betegségek
HIV-fertőzés
NCT-szám
NCT07226128

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 150
  • 2026. ápr. 10. és az elsődleges befejezés (2029. aug. 31.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Active suicidality at Entry, as determined by the patient's HIV provider or social worker following a positive response (1, 2, or 3) to PHQ-9 Item #9 and a positive response (yes) to one or more of the three questions (for Question #3, the previous attempt must be within the past 10 years) on the Patient Suicidality Form (see Appendix).
  • Therapy for serious medical illnesses within 14 days prior to the Entry Visit
    • NOTE: Therapy for serious medical illnesses that overlaps with a study visit will result in postponement of that study visit until the course of therapy is completed; postponement outside of the allowed study visit timeframe will result in study discontinuation.
  • Receipt of investigational agents, cytotoxic chemotherapy, systemic immunosuppressive therapies, systemic glucocorticoids (of any dose), or anabolic steroids at the Entry Visit
    • NOTE: Physiologic testosterone replacement therapy or topical steroids is not exclusionary. Inhaled/nasal steroids are not exclusionary as long as the participant is not also receiving HIV protease inhibitors
    • NOTE: Use of NSAIDS and aspirin are allowed
  • Active drug use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements.

Más betegség

  • History of bipolar disorder or a psychotic disorder, including schizophrenia
    • NOTE: Depressive disorders are not exclusionary.
  • Diagnosed disease or process, besides HIV infection, associated with increased systemic inflammation (including, but not limited to, systemic lupus erythematosus, inflammatory bowel diseases, or other collagen vascular diseases).
    • NOTE: Hepatitis B or C co-infections are NOT exclusionary, but treatment for hepatitis C cannot be provided during study participation
  • End stage renal disease requiring renal replacement therapy (dialysis, transplantation).
  • Known or suspected malignancy requiring systemic treatment within 180 days of the Entry Visit.
    • NOTE: Localized treatment for skin cancers is not exclusionary.

Laborértékek

  • Diagnosed diabetes mellitus or any previously recorded HbA1c ≥6.5%

Egyéb

  • Inability to complete written, informed consent
  • Inability to read and understand English as seen on a computer screen
  • Incarceration at the time of any study visit
  • Pregnancy or breastfeeding during the study.

Kiket keres a vizsgálat

  • HIV-1 infection, documented as listed clinically in the participant's electronic medical record by any of the following tests: (1) any licensed rapid HIV test, (2) HIV enzyme test kit at any time prior to study entry, (3) at least one detectable HIV-1 antigen, or (4) at least one detectable plasma HIV-1 RNA viral load.
  • Age ≥ 18 years.
  • Ongoing receipt of stable antiretroviral therapy of any kind for at least 180 days prior to Screening
  • Meets the depression definition for this trial:
    • (1) repeat PHQ-9 ≥10100 result at the Screening Visit (suggesting moderate to severe depressive symptoms), AND
    • (2) PHQ-9 depressive disorder diagnosis (2 or more of the 9 depressive symptoms, including depressed mood or anhedonia, present in the past 2 weeks), AND
    • (3) functional impairment (using the tenth PHQ-9 item assessing social/occupational impairment), AND
    • (4) no evidence that the direct physiological effects of a substance, medication, or medical condition clearly account for the depressive symptoms, AND
    • (5) no bipolar or psychotic disorders
    • NOTE: The use of antidepressant medications is not exclusionary.
  • HbA1c < 6.5% at Screening
  • HIV-1 RNA level < 75 copies/mL at Screening
    • NOTE: There are no CD4 cell count eligibility criteria for this trial.

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
Indiana University HealthIndianapolisEgyesült ÁllamokToboroz

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