Collecting Information About Treatment Results for Patients With Cushing's Syndrome

Part of paid clinical trials in Basking Ridge, New Jersey.

Sponsor
Memorial Sloan Kettering Cancer Center
Study ID
NCT03364803
Status
Recruiting

Conditions

  • Cushing Disease
  • Cushing Syndrome
  • Cushing's Disease

Eligibility Criteria

Sex
ALL
Age
14 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Cushing's QoL (Quality of Life Questionnaire) — OTHER
    Cushing's QoL is a validated disease specific questionnaire consisting of 12 questions on a five-point Likert scale ranging from always to never. The total score ranges from 12 to 60, with a lower score indicating a greater negative impact on health related QoL. This is converted to a 0-100 scale, 0 indicating the worst and 100 indicating the best QoL
  • Nottingham Health Profile (NHP) — OTHER
    NHP is used in patients to assess general health and quality of life. This assessment consists of 38 yes/no questions that are subdivided into six scales assessing impairments: pain (eight items), energy level (three items), sleep (five items), emotional reactions (nine items), social isolation (five items) and physical mobility (eight items). A higher score indicates more impairment
  • Hospital Anxiety and Depression Scale (HADS) — OTHER
    HADS consists of 14 items pertaining to anxiety and depression, with each item measured on a four-point scale. Total scores for the anxiety and depression subscales range from 0 to 21. A higher score indicates greater symptomatology
  • Perceived Stress Scale (PSS) — OTHER
    The PSS predicts both objective biological markers of stress and increased risk of disease in patients with higher stress levels.
  • Barratt's Impulsivity Scale (BIS) — OTHER
    BDI and BIS in combination have demonstrated that depression and/or binge eating may be mediating factors for the outcome of obesity
  • Beck Depression Inventory (BDI) — OTHER
    BDI and BIS in combination have demonstrated that depression and/or binge eating may be mediating factors for the outcome of obesity
  • State-Trait Anxiety Inventory (STAI) — OTHER
    The STAI provides data to help distinguish between anxiety and depression.
  • State Food Craving Questionnaire-State (FCQ-S) — OTHER
    The FCQ-S consists of 15 items assessing: desire to eat, anticipation of positive reinforcement from eating, anticipation of negative reinforcement (reduction of negative affect) from eating, lack of control over eating, and (physiological) hunger; higher scores reflect stronger food craving. Participants respond, using a Likert-type scale, how much each item is true of them right now.
  • Trait Food Craving Questionnaire-Trait (FCQ-T) — OTHER
    Trait food craving will be assessed with the Food Craving Questionnaire-Trait (FCQ-T). The FCQ-T consists of 39 items assessing: intentions/plans to eat, anticipation of positive reinforcement from eating, anticipation of negative reinforcement from eating, lack of control over eating, preoccupation with food, (physiological) hunger, emotions preceding or following food cravings or eating, environmental cues that may elicit food cravings, negative emotions including guilt experienced as a consequence of food cravings, and/or indulging such cravings; higher scores again indicate higher trait craving. Individuals are asked to respond, using a Likert-type scale, how much each item is true of them in general.
  • Visual Analogue Scale (VAS) — OTHER
    A validated visual analogue scale (VAS) questionnaire will be completed in the fasting state. The VAS consists of 100-mm lines with words anchored at each end describing extreme sensations of hunger, prospective consumption ("How much do you think you can eat?"), fullness, and satisfaction, as well as craving (sweet, salty, fatty or savory). Patients will be asked to make a vertical mark across the line corresponding to their feelings. Quantification will performed by measuring the distance from the left end of the line to the mark.
  • Sensitivity to Reinforcement of Addictive and other Primary Rewards (STRAP-R) food variant — OTHER
    A validated questionnaire that assesses perceived subjective value attributed to expected/hypothetical foods and other primary reinforcers will be administered. This variant of this questionnaire was initially developed by Dr. Goldstein to assess 'liking' and 'wanting' of expected drug rewards for patients with cocaine addiction. The current assessment uses a modified version to assess 'liking' and 'wanting' for food.

Study Details

The purpose of this study is to follow participants with Cushing's syndrome during the course of their routine care and to form a data registry to study long term participant outcomes.

Key Dates

Start date
Nov 28, 2017
Status verified
Oct 2025
Primary completion
Nov 28, 2026
Completion
Nov 28, 2026

Study Design

Enrollment
300 participants (estimated)

Arms

  • Arm: Participants with Cushing's Syndrome

Primary Outcome Measure

Collection of data on Cushing's Syndrome participants before and over time after surgical, medication, and/or radiation therapy. [ Time Frame: up to 10 years after treatment ]

Central Contacts

Locations (7)

FacilityCityStateZIPSite coordinators
Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)Basking RidgeNew Jersey07920
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)MiddletownNew Jersey07748
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Bergen (Limited Protocol Activities)MontvaleNew Jersey07645
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited protocol activity)CommackNew York11725
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Westchester (Limited Protocol Activities)HarrisonNew York10604
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Cancer CenterNew YorkNew York10065
Eliza Geer, MD
646-888-2627
Memorial Sloan Kettering Nassau (Limited Protocol Activities)UniondaleNew York11553
Eliza Geer, MD
646-888-2627

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