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Treatment of Eating Disorders by Physical Activity and Nutrition Counseling

Treatment of Eating Disorders - a Randomised, Controlled, Prospective Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02079935
Acronym
FAKT
Enrollment
128
Registered
2014-03-06
Start date
2014-03-31
Completion date
2019-01-31
Last updated
2019-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bulimia Nervosa, Binge Eating Disorder

Keywords

BN, Binge, overconsumption of food, purging, purge

Brief summary

Eating disorders includes anorexia nervosa, bulimia nervosa, binge eating and other specified feeding or eating disorder (OSFED). Common to all is the intensively occupation to control food intake, body image and body weight. Most people with this kind of disorder don't reach for professional help, or there may be more than 4 years before they do. Cognitive behavior therapy is the foremost method of treatment of eating disorders, but up to 30-50% of the patients don't respond to this. The investigators find it important to identify science based alternatives of therapy, as this may reduce the health concern, and broaden the choice of therapy methods. A former study by Sundgot-Borgen et al in 2002, found guided physical activity to reduce symptoms of bulimia nervosa just as good as the traditional cognitive therapy. The primary objective of the project is to see whether the combination of physical exercise and dietary therapy is more effective in treating eating disorders, than cognitive therapy. Secondly, the investigators want to see whether there are any differences with regard to the individual satisfaction of treatment method, and to associated costs. Interviews with a sufficient number of participants from the PED-t arm to meet data saturation criteria, and all theraphists in the new treatment offer, will give uniqe insight to experiences with the treatment method and the delivery of treatment.

Detailed description

Subjects are recruited through primary doctors, social media and newspapers, and will be included continuously by screening interviews. There will be a randomization into two treatment groups (cognitive behavior, or physical activity and nutrition education) to be followed for 16 weeks. Each week includes one meeting of group therapy (90 minutes) and homework related to treatment, and for 4 weeks midway there will be two therapy meetings pr week (a total of 20 meetings). Post tests are planned at week 17, and at 6, 12, and 24 months after treatment. Participants reqruited during ongoing treatment groups are placed on a waitlist, serving as controls to the treatment groups.

Interventions

Following group-modified protocol for cognitive behavioral therapy, CBT, first described by Fairburn 2008, modified by Modum Bad, Norway.

BEHAVIORALPhysical Activity and Dietary Therapy

Guided physical activity and dietary therapy, to (re-)introduce a more healthy lifestyle and help stabilizing a healthy weight. A detailed manual will be published.

Sponsors

The Norwegian Women´s Public Health Association
CollaboratorOTHER
University of Tromso
CollaboratorOTHER
Norwegian School of Sport Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The one transferring results from lab's and questionaires to SPSS are blinded for group affiliation.

Intervention model description

Comparing treatment of cognitive behavioural therapy, with treatment of physical exercise and dietary therapy. All participants randomized to either of the two treatment offers. Waitlist serves as control group.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Women, * BMI 17,5-35, * Age of 18-40 years, * DSM-5 criteria of bulimia nervosa, * DSM-5 criteria of Binge eating disorder * Living nearby Norwegian School of Sports Sciences, NSSS, in Oslo (Norway)

Exclusion criteria

* Age \<18 and \>40 years * BMI \<17,5 and \>35 * Pregnancy * Competing/experienced athlete * Anorexia nervosa * Currently, or during the past 2 years, in active treatment with cognitive therapy * Other personality disturbances * Suicidality

Design outcomes

Primary

MeasureTime frameDescription
Effectiveness of treatment, evaluated through the change in symptoms of eating disorderPre-test in week 0, Post-tests (week 17), and at 6, 12, and 24 months after intervention.Change in ED-symptoms are evaluated through screening and surveys: EDE-questionaire (Episodes of binge eating, episodes of purging, concern for body weight and appearance)(Fairburn, 2008), Clinical Impairment Assessment (CIA) (Fairburn, 2008), Eating Disorder Inventory-3 (EDI) (Garner, 2004), Eating Disturbance Scale (EDS-5) (Rosenvinge et al., 2000), DSM-5 (APA, 2013)

Secondary

MeasureTime frameDescription
Experiences of the treatment method for eating disordersPost-test (week 17)Interview on the experiences the patients have to the specified treatment method of eating disorders (arm of intervention), EPDEX (Clinton 2001)
Associated cost with treatment methodPre-testCalculation of the directly and indirectly cost related to treatment method
Associated cost With treatment methodPost-test (by 6th month post-treatment)Calculation of the directly and indirectly cost related to treatment method
Expectations of treatment method for eating disordersPre-testInterview on the expectations the patients have to the specified treatment method of eating disorders (arm of intervention) EPDEX (Clinton 2001)
Group climateweek 1-16coerciveness scale from Therapeutic Factor Inventory (Lese & MacNair-Semands, 2000).
Working AIlianceweek 1-16Working AIliance Inventory (Horwath & Greenberg, 1989)
Change in eating disorder behavior and cognitions related to body figure and bodyweightWeek 1-16 during treatmentEvaluation after each therapy session on progress in reducing eating disordered behaviour (binging and purging) and on changes of cognitions on body figure and -weight
Global measurement of general psychopathologyPre-treatmentBeck's Anxiety Inventory (BAI), Beck Depression Inventory (BDI), QoL (Diener), Utrecht Coping List, Resilience Scale for Adults, the outcome rating scale (ORS), the three-factor eating questionnaire (TFEQ), Binge eating Scale (BES), Cantril's Ladder, Exercise dependency test, compulsice exercise test

Other

MeasureTime frameDescription
Interview: What are the theraphists experiences of their contribution to the PED-t programPost treatmentQualitative approaches, such as in-depth interviews, will give additional insights into the therapists' perspectives and experiences on delivering a new treatment offer for eating disorder. Data are analyzed in four steps within the framework of systematic text condensation (Malterud 2012).
Change in muscular strengthPretest (week 0), post-test (week 17) and at 6, 12 and 24 months after treatmentStatus of 1 repetition maximum, 1RM, muscular strength in squats, bench press and seated row
Interview: What are the experiences of the participants who drop out of the PED-t program?Post treatmentData are analyzed in four steps within the framework of systematic text condensation (Malterud 2012).
Change in cardiovascular endurancePre-test in week 0, Post-tests ( week 17), and at 6, 12 and 24 months after intervention.CPET: with the use of modified Balke Treadmill performance evaluation test, The Borg scale (Borg, 1982)
Change in bone mineral densityPre-test in week 0, Post-test (week 17) and 6, 12, and 24 months post-treatmentDXA (Dual-energy X-ray absorptiometry)
Change in body weight and bodycompositionPre-test and post-test (week 17) and at 6,12,18 and 24 months post-treatmentDXA (dual-energy x-ray absorptiometry) (weekly weight registration will also be kept in each arm of treatment)
Change in nutritional statusPre-test, in week 8 of treatment, post-test (week 17) and at 6,12,18 and 24 months post-treatmentBlood test to identify nutritional status of iron, folate, cholesterol and triglycerides, ApoA, ApoB and vitamin-D, folic acid
Change in hormonal statusPre-test, week 8 of treatment, post-test (week 17) and at 6,12,18 and 24 months post-treatmentBlood test to evaluate hormonal status of estradiol, progesterone, CTX, P1nP, insulin, leptin, TSH, T3, T4, FSH, LH, cortisol
Change in dietary and nutritional intakePre-test, each 3rd week in treatment (a total of 5 interviews), post-test (week 17), and post-treatment (6,12, and 24 months post-treatment)24 hour recall interview: interview on the intake of food and beverage during the past 24 hours.
Change in physical activity levelPre-test in week 0, Post-test (week 17) and 6, 12, and 24 months post-treatmentWearing a GT3X-BT actigraph accelerometer for 7 consecutive days and making notes on daily activity in 30 minutes intervals
Interview: measure and explore patients experienced treatment satisfaction and outcome/benefits with PED-t.Post treatmentQualitative approaches, such as in-depth interviews, will give additional insights into ED-patients' perspectives, notably experiences and satisfaction with the treatment. A sufficient number of participants to meet data saturation criteria are qualitatively interviewed. Data are analyzed in four steps within the framework of systematic text condensation (Malterud 2012).

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026