Efficacy of a Positive Psychological Intervention in Patients With Eating Disorders

Sponsor
Universitat Jaume I (Other)
Overall Status
Completed
CT.gov ID
NCT03003910
Collaborator
Hospital Provincial de Castellon (Other), PREVI Clinical Center (Other)
54
1
2
33
1.6

Study Details

Study Description

Brief Summary

This study is aimed to test the efficacy of a positive psychological intervention for promoting positive emotions and optimistic thinking in eating disordered patients. Participants are randomly assigned to receive the positive intervention or the control condition, which consists on thinking about daily activities.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Best Possible Self
  • Behavioral: Daily Activities
N/A

Detailed Description

Eating disorders (ED) are very difficult conditions to treat. Therefore, interventions in this field are shifting their main target towards the disorder's impact in quality of life, rather than ED symptomatology in itself. In this sense, a focus in the promotion of positive emotions and well-being is emerging in order to buffer from the harmful effects caused by ED.

Positive psychological interventions have shown efficacy in the promotion of positive emotions and well-being. In this sense, one of these interventions is called Best Possible Self (BPS), since is aimed to enhance positive emotions and well-being. Specifically, BPS is a positive future thinking technique, which requires people to envision themselves in the future, after everything has gone as good as it possibly could. This exercise has shown efficacy improving optimism, future expectancies and positive affect compared to a control condition, in general population and depressive patients.

Furthermore, the progress of Information and Communication Technologies, has allowed the development of technology applications and devices that could enhance the quality of experience and the well-being levels. This approach is called Positive Technology and it can be used as a complement to positive psychological interventions. Positive Technology can be defined as the scientific and applied approach to improve the quality of our personal experience trying to increase wellness and generate strengths.

Taking into account the prior literature, the aim of the present study is to carry out a randomized controlled study with ED patients in order to explore if BPS is able to produce improvements in different well-being and clinical measures. The exercise will be applied through a Positive Technology system. The design employed in this study is similar to the used in other studies.

Five assessment moments were used: Before the exercise (baseline), after the first session (day 1) and post-training (1 month). Moreover, two follow-ups were included: one month after finishing the training period (1st follow-up) and three months after finishing the training (2nd follow-up)

Study Design

Study Type:
Interventional
Actual Enrollment :
54 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Efficacy of a Positive Psychological Intervention in Patients With Eating Disorders: a Randomized Control Trial
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Nov 1, 2015
Actual Study Completion Date :
Nov 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Best Possible Self

Participants are asked to write and imagine about a future in which they have reached all their goals and they have developed all their potentialities in four different domains: personal, professional, social and health domain. They carry out the exercise in a Positive Technology System called the "Book of Life", which has shown efficacy in the enhancement of positive mood (Baños, Etchemendy, Farfallini, García-Palacios, Quero & Botella, 2014). This application looks like a personal diary, where participants can write all that they want and these essays are supported by multimedia content (pictures, songs and videos). Additionally, they can continue doing the exercise in a web platform in which they can visualize all the content they had developed previously.

Behavioral: Best Possible Self
Intervention group which requires people to envision themselves in a future in which all has gone in the best possible way.
Other Names:
  • Positive Psychological Intervention
  • Placebo Comparator: Daily Activities

    Participants are asked to think and write about all that they have done the last 24 hours. They carry out the exercise in a powerpoint document, where they can record all the activities, situations and thoughts occurred in the past 24 hours.

    Behavioral: Daily Activities
    Control group which consists of thinking and writing about all the activities and situations that had taken place during the last 24 h.

    Outcome Measures

    Primary Outcome Measures

    1. Subjective Probability Task (SPT; MacLeod, 1996). Change assessment. [Baseline, day 1, 1 month, 2 months, 4 months]

      This scale measures positive and negative expectancies about future events. It consists of 20 statements referring to negative expectancies and 10 statements referring to positive expectancies. Participants answer on a 7-point scale (Not at all likely to occur - Extremely likely to occur). Some studies have found an appropriate levels of internal consistency for positive and negative expectancies (α=0.80-0.82 y 0.91, respectively).

    2. Positive and Negative Affect Scale (PANAS, Watson, Clark & Tellegen, 1988; Sandín et al., 1999). Change assessment. [Baseline, day 1, 1 month, 2 months, 4 months]

      To measure affect, the Spanish adaptation of the Positive and Negative Affect Scale was used (PANAS, Sandín et al., 1999; Watson, Clark & Tellegen, 1988). This instrument is composed of 20 items: 10 items measuring positive affective states and 10 items measuring negative affect states. Participants rate on a five-point scale (from "Not at all" to "Extremely") the degree to which they usually feel a specific affective state. PANAS is one of the most widely-used instruments to measure affect because it shows excellent psychometric properties (Cronbach Alpha's from 0.87-0.91).

    Secondary Outcome Measures

    1. Life Orientation Test (Lot-R; Otero, Luengo, Romero Gómez & Castro, 1998; Scheier, Carver & Bridges, 1994). Change assessment. [Baseline, 1 month, 2 months, 4 months]

      This scale measures positive and negative expectancies about future events. It consists of 20 statements referring to negative expectancies and 10 statements referring to positive expectancies. Participants answer on a 7-point scale (Not at all likely to occur - Extremely likely to occur). Some studies have found an appropriate levels of internal consistency for positive and negative expectancies (α=0.80-0.82 y 0.91, respectively).

    2. General Self Efficacy Scale-12 (GSES-12; Bosscher et al., 1997; Herrero et al., 2014). Change assessment. [Baseline, 1 month, 2 months, 4 months]

      This questionnaire evaluates a general dimension and three aspects of self-efficacy: initiative, persistence and effort. The internal consistency coefficients for the subscales varied from excellent to good (Initiative = 0.83; Effort =0.77; Persistence = 0.80; and Total = 0.86).

    3. Dispositional Hope Scale (DHS; Snyder et al., 1991). Change assessment. [Baseline, 1 month, 2 months, 4 months]

      This instrument evaluates dispositional hope. It is composed of 12 items (Agency: 4 items; Pathways= 4 items; Fillers= 4 items), with an 8-point Likert scale ranging from 1 (definitely false) to 8 (definitely true). Internal consistency coefficient (Cronbach's alpha) for the total scale was excellent (.89).

    4. Self-Concordant Motivation (SCM; Sheldon & Elliot, 1999) [day 1]

      This instrument assesses participants' initial motivation to do the assigned exercise. It explores the different reasons for the participants to carry out the exercise. The scale is composed of 4 items whose goal is to find out whether the motivation is intrinsic or extrinsic. A total score is obtained by subtracting the two extrinsic motivation scores from the two intrinsic motivation scores.

    Other Outcome Measures

    1. Eysenck Personality Questionnaire - Revised - Neuroticism (EPQ-R-N; Eysenck, Eysenck & Barrett, 1985; Eysenck & Eysenck, 1997). [Baseline]

      This scale assesses the neuroticism level of the individual, showing if he is stable or neurotic. This subscale is composed by 12 items of dicotomic response (yes-not). Regarding psychometric properties, Eysenck and Eysenck (1997) got an alpha coefficient between 0-73 and 0.82.

    2. Eating Attitudes Test (EAT-26; Garner, Olmsted, Bohr & Garfinkel, 1982) [Baseline]

      This questionnaire assesses a broad range of attitudes and behaviors related to anorexia nervosa. It is composed of 26 items rated on a 6-point Likert scale from 0 (never) to 6 (always), based on the frequency with which the individual carries out the behavior or has the thought described by the item. The instrument has shown excellent psychometric properties (Toro, Castro, Garcia, Perez & Cuesta, 1989; Rivas, Bersabé, Jiménez & Berrocal, 2010).

    3. Brief Symptom Inventory (Ruipérez, Ibañez, Lorente, Moro & Ortet, 2001) [Baseline]

      This scale encompass ninve primary dimensions of psychopathological symptoms: psychoticism, somatization, depression, hostility, phobic anxiety, obsessive-compulsive, anxiety (panic), paranoid ideation, and nervous tension. Each BSI item is rated on a 5- point scale (0 to 4) according to manifestations of symptoms in the last 30 days (ranging from "not at-all" to "extremely").

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subject has a diagnosis of Eating Disorder by a Clinical Psychologist according to DSM-IV criteria

    • Subject accepts to participate in the study voluntarily

    Exclusion Criteria:
    • Subject suffering a severe physical condition

    • Subject suffering from substance or alcohol depedence

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Jaume I Castellón Spain 12006

    Sponsors and Collaborators

    • Universitat Jaume I
    • Hospital Provincial de Castellon
    • PREVI Clinical Center

    Investigators

    • Study Director: Cristina Botella, Professor, University Jaume I

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Angel Enrique Roig, Ph.D Student, Universitat Jaume I
    ClinicalTrials.gov Identifier:
    NCT03003910
    Other Study ID Numbers:
    • aenrique
    First Posted:
    Dec 28, 2016
    Last Update Posted:
    Dec 28, 2016
    Last Verified:
    Dec 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Angel Enrique Roig, Ph.D Student, Universitat Jaume I
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 28, 2016