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Anorexia NervosaNCT05861661

Social Cognition in Patients With Anorexia Nervosa- the Study Examines Social Understanding in Patients With AN Via Questionnaire and Computer Tasks

An observational study of Anorexia Nervosa, run by Ziv Hospital at 2 sites in Israel.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The current research has two goals: first to validate the Hebrew version of a new measurement for assessing mentalization failures. The second goal is to examine the connection between attachment, emotional regulation strategies, mentalization, and specific mentalization failures - As they manifested in anorexia… Read more about this study

Who is it for?
Ages 16 to 28 years, women onlyHealthy volunteers can take part
Conditions the study is for
Anorexia Nervosa
What is being tested?
The study do not include an intervention
How many people
60 participants
Where
2 sitesIsrael
Study dates
12 Jul 2020to 12 Jul 2021
How long will I take part?
6 Months
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 to 28 years
  • Women only
  • Healthy volunteers accepted
  • Child, Adult

Study population: Women hospitalized with AN at the ages 16-28.

Who may be able to join

  • All patients will meet the DSM-5 (APA, 2013) criteria for diagnosis of AN on admission.

Who cannot join

  • Patients will have no lifetime or current diagnosis of bipolar disorder, schizophrenia spectrum disorder, substance use disorder, mental retardation, organic brain syndrome, and any physical disorder except for inter-current medical problems.

Trial locations and contacts

2 sites in 1 country.

Israel2 sites
  • Sheba Medical Center

    Ramat Gan, 32205

  • Ziv Hospital

    Safed, Galilee, 13100

Other trials in Israel

About this study

Official title: The Connection Between Attachment, Emotional Regulation and Mentalization Failures in Anorexia Nervosa

The current research has two goals: first to validate the Hebrew version of a new measurement for assessing mentalization failures. The second goal is to examine the connection between attachment, emotional regulation strategies, mentalization, and specific mentalization failures - As they manifested in anorexia nervosa (AN) compared with non-patient controls. The study includes computer tasks, questionnaires and two short tasks administrated by the examiner.

Read the detailed description

Study goals:

  1. To validate the Hebrew version of the Movie for the Assessment of Social Cognition (MASC) which asses mentalization ability and mentalization failures (Dziobek et al., 2006). This version of the MASC was recently designed by the study group in Haifa University. The validation of this version of the MASC will be done by comparing patients with AN to non-patients.
  2. To examine the connection between attachment styles, emotional regulation strategies, mentalization, and specific mentalization failures.

Study Hypotheses:

  1. In respect to the first goal of the study, we hypothesize that a. a significant correlation between the MASC and other tools examining different aspects of mentalization (RME, CAM, TAS and RFQ) will be fond; b. different patterns of mentalization will be found between the clinical group and the control group on the MASC. More specifically, patients with AN will show more hypo-mentalization tendencies on the MASC then the control group.
  2. regarding the second goal of the study, we hypothesize that the connection between attachment and mentalization failures will be mediated via emotional regulation strategies. More specifically, we anticipate that the connection between avoidant attachment and hypo-mentalization will be mediated via emotional isolation strategy and the connection between anxious attachment and hyper-mentalization will be mediated via emotional flood.

Method:

Participants This study will include 120 participants at the ages of 16-26. The participants will be assigned into two groups. The AN group will include 60 women diagnosed according to the DSM-5 (APA, 2013) as suffering from AN and are currently hospitalized. The control group will include 60 women participants, which will be screened and excluded if found to be suffering from any type ED, have a psychiatric background or any chronic disease. The control group will be recruited threw Haifa university. The control group session will take place in Haifa university.

Measures

Measures of mentalization

The Movie for Assessment of Social Cognition (MASC) (Dziobek et al., 2006) - Hebrew version. This task was designed to serve as a refined, easily-administered, ecologically-valid measure of ToM and ToM errors. It was originally shown to discriminate between adults with Asperger syndrome and healthy controls, and has since been used in studies researching ToM, mentalization and mentalization deficits in different psychopathology's, including AN and SAD. It was also translated to Spanish and Norwegian, and was found to be valid in these languages (Lahera et al., 2014, Fretland et al. 2015). The task consists of a film depicting four young adults getting together for dinner. The film stops at various points to pose questions regarding the thoughts, intentions and feelings of the characters. Overall, the task includes 45 multiple-choice questions; each question has one correct answer and three distractors, which can be characterized as reflecting exceeding ToM/hypermentalization, insufficient ToM/hypomentalization and concrete answers which involve no ToM. We will use the Hebrew version of the task, which was translated and dubbed for the purpose of the current research project.

Reading the Mind in the Eyes (RME)- Revised Version (Baron-Cohen et al., 2001). This task was designed to assess the ability to recognize basic and complex emotions and ToM. It has also been found to be valid when translated into other languages (Hallerbäck et al., 2009, Prevost et al., 2014). In the current study we will use the Hebrew version translated by Milo. During the task, participants are presented with 52 photographs of eyes exhibiting basic emotions (happy, sad, afraid, surprised, disgusted, angry) (Ekman \& Friesen, 1976) as well as complex emotions (interested, worried, confident, fantasizing, preoccupied, friendly and suspicious) (Baron-Cohen et al., 1997). Each picture is presented twice, and participants are asked to make a forced choice between four words naming the emotion, with only one correct answer.

The Cambridge Mindreading (CAM) Face-Voice Battery - (Golan et al., 2006). This battery examines complex emotion and mental-state recognition in both visual and auditory format. In the current study we will use only the visual task, which is comprised of silent clips of adult actors, both male and female, of different ethnicities, expressing emotions facially. Fifty faces examine recognition of 20 different complex emotions and mental states (e.g., intimate, insincere). During each trial, a clip is presented and the participants are asked which of four words best describes the emotions being displayed. There is no time limit for answering. The battery provides an overall facial emotion recognition score (max =50) as well as individual scores for each of the 20 emotions assessed (pass/fail, i.e., recognized above chance or not) and an overall number of the emotions correctly recognized (max=20). The current study will use a Hebrew version of this task which was developed by Prof. Ofer Golan, one of the designers of the original English version, alongside Prof. Lily Rothschild-Yakar.

The Toronto Alexithymia Scale (TAS-20) - (Griffith, 1998). The TAS is a 20-item self-report measure, which was developed for the assessment of alexithymia, yet can also be used to measure mentalization in relation to the self (Luyten et al., 2012). The scale has 3 factors which were confirmed in several studies (Parker, Taylor, \& Bagby, 2003): (a) difficulty in identifying feelings, (b) difficulty in describing feelings to others; and (c) externally oriented thinking. The scale's internal consistency (α =.81(, and test-retest reliability (r = .77) have been established (Bagby, Taylor, \& Parker, 1994), and its Hebrew version showed good internal consistency (α = 0.89; Rozenstein et al. 2011) The Reflective Functioning Questionnaire (RFQ), (Fonagy et al, 2016). The RFQ is a relatively new instrument, developed as a brief, easy-to-administer, self-report screening measure of mentalization. It originally included 46 items which the participant responded to on a 6-point scale. Factor analysis yielded two main factors, assessing Certainty (RFQ_C) and Uncertainty (RFQ_U) about the mental states of self and others. These two factors allow distinguishing between the two the main mentalization impairments, hyper-mentalization and hypo-mentalization, with high scores of certainty indicating hyper-mentalization and high scores of uncertainty reflecting hypo-mentalization; low scores on both scales indicate more genuine mentalizing. The factors were relatively distinct, invariant across clinical and non-clinical samples, had satisfactory internal consistency and test-retest stability, and were largely unrelated to demographic features. The questionnaire's developers have since designed a short, 8-item version, consisting of the highest loading items on their respective factor as seen in exploratory and confirmatory factor analyses. We will use the short Hebrew version supplied by the questionnaire's authors.

Measure of attachment

Experiences in Close Relationships Scale (ECR), (Brennan et al., 1998). This measure examines patterns of attachment through a self-report questionnaire containing 36 items. The participants are required to rate to what extent each item describes his attitude toward close relationships, from (1) - strongly disagree, to (7) - strongly agree. 18 items relate to an insecure/anxious attachment pattern, and another 18 items relate to an insecure/avoidant attachment pattern. The original study reported Cronbach's alpha as .91 and .94 for the Anxiety and Avoidance subscales, respectively, and similar results have been found since (Vogel \& Wei, 2005). Test-retest reliability has been shown to be around 0.7 (Lopez \& Gormley, 2002). The Hebrew version of the questionnaire will be used in this study, translated by Mikulincer \& Florian (2000). They also validated its two-factor structure on an Israeli sample, with high internal reliability (Cronbach's alpha .92 for anxious attachment and .93 for avoidant attachment).

Measure of emotion regulation The Differentiation of Self Inventory (DSI), (Skowron \& Friedlander, 1998; Skowron \& Schmitt, 2003). The DSI is a self-report questionnaire that measures self-other differentiation as well as adaptive emotional regulation, which are vital for the development of mentalizing ability. This is a self-report instrument for adults (age ≥25 years), that was modification translated to Hebrew and validated for adolescents and young adults (Rothschild-Yakar et al., 2016). We will use the Hebrew version of Skowron and Schmitt's (2003) revised edition comprising 46 items in four subscales (Emotional Reactivity, I Position, Emotional Cutoff and Fusion with Others). Participants rated items on a 6-point Likert-type response scale ranging from Not at all (1) to Very true (6). Higher scores indicate a greater level of differentiation. The DSI showed external validity, with elevated DSI scores predicting lower chronic anxiety and better psychological adjustment (Skowron \& Friedlander, 1998). Internal consistency reliabilities of the DSI and its subscale calculated with Cronbach's alpha were reported as follows: DSI full scale=.88, Emotional Reactivity=.84, I Position=.83, Emotional Cutoff=.82, and Fusion with Others=.74 (Skowron \& Friedlander, 1998).

Measures of background variables, comorbidity, and estimation of intellectual ability

Personal details questionnaire. This questionnaire covers basic personal details such as age, country of origin, formal education, past or present emotional difficulties, past or present symptoms of EDs and the height and weight of the participants, as well as family details such as parental marital status, socioeconomic status, and parental education.

The short Depression, Anxiety and Stress Scale (DASS)-21 - (Lovibond \& Lovibond, 1995). The DASS-21 is a 21-item self-report measure designed to assess and discriminate between symptoms of depression, anxiety, and stress. It consists of 21 items, which participants rate on a scale of 0 to 3 about how accurately statements regarding depression, anxiety, and stress applied to them over the past week. The DASS-21 has demonstrated acceptable psychometric properties in clinical and nonclinical populations, with high internal consistency for each sub-scale ranging from α = .82 to .94 (Antony, Bieling, Cox, Enns, \& Swinson, 1998; Henry \& Crawford, 2005).

The Eating Attitudes Test (EAT-26): (Garner et al, 1982). The EAT-26 will be used to measure the presence and severity of EDs. This is a self-report questionnaire that examines the level of pathological eating-related preoccupations and behaviours. The EAT-26 includes three main subscales: (a) dieting, refraining from fatty food, and physical appearance; (b) bulimic symptomatology and preoccupation with food; and (c) personal control over eating habits. Participants rate the 26 items on a 6-point scale ranging from Never (1) to Always (6). High reliability and validity of the EAT-26 were found across different cultures (Garfinkel \& Newman, 2001; Garner et al 1982), including in Israeli patients with EDs (Koslowsky et. al., 1992, Niv-Nadler, 1997).

The SCOFF- questionnaire for the assessment of eating disorders (Morgan et al., 1999). The SCOFF questionnaire is a simple 5- yes/no question tool, developed to screen for eating disorders in the general population. For every positive answer one point is given. A total score of two and above has been found to be 100% sensitive and 87.5% specific for the presence of any ED.

An estimated IQ: Similarities and block design subtests (Wechsler, 2008). Similarities and Block Design will be used as an estimate for IQ. The Similarities and Block Design subtests will be used from the Hebrew version of WAIS IIIHeb (Wechsler, 1997) for Adults. The two subtests were found to possess high loading on the factors to which they belong (Watkins et al, 2006).

Study procedure All tasks will be administrated individually by a master or doctoral student in a single two hours session. After receiving an information regarding the purpose of the study and its procedure the participants will sign a consent form. For participants under the age of 18, parental consent will be obtained as well. During the session the participants will complete online self-report questionnaires (personal details questionnaire, experiences in close relationships scale and the differentiation of self inventory) followed by the Hebrew version of the movie for assessment of social cognition (MASC-heb). Then the participants will complete an online self report questionnaire ( the Toronto alexithymia scale) followed by two computer tasks (the Cambridge mindreading face-voice battery and the reading the mind in the eyes),the Wechsler's Similarities and Block design and more online self- report questionnaires (the short depression, anxiety and stress scale, the reflective functioning questionnaire and the eating attitudes test 26).

To ascertain that the participants of the control group will not include participants suffering from EDs, they will pass the SCOFF questionnaire which is a common screening tool for Eds.

Control participants will be compensated for their participation by 80 NIS for their participation in the study. Control group sessions will take place in Haifa university.

20 participants (10 from the AN group and 10 from the control group) will be invited to a second half hour session, 2-6 month after the first session. The session will be administrated by a master or doctoral student. After receiving an information regarding the purpose of the study and its procedure the participants will sign a consent form. For participants under the age of 18, parental consent will be obtained as well. During the session the participant will complete the MASC-heb. Control participants will be compensated for their participation by 40 NIS for their participation in the study.

Being tested
The study do not include an intervention
Medical subject headings
Anorexia Nervosa

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • The study do not include an interventionOther

    The study do not include an intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mentalization impairments measured by questionnaire

    Measured: one year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 May 2023
  2. Study start12 Jul 2020
  3. Primary completion12 Jul 2021
  4. Study completion12 Jul 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
60 participants (actual)
Target duration
6 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT05861661
Sponsor's protocol ID
0051-20-ZIV
Status last verified
Jul 2020
First submitted
12 Jul 2020
Last updated
17 May 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Anorexia Nervosa, run by Ziv Hospital at 2 sites in Israel.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 May 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mentalization impairments measured by questionnaire (time frame: one year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 May 2023.

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