---
title: Self-Help And Recovery Guide in Eating Disorders
nct_id: NCT02336841
overall_status: UNKNOWN
phase: EARLY_PHASE1
sponsor: "King's College London"
study_type: INTERVENTIONAL
primary_condition: Anorexia Nervosa
countries: United Kingdom
canonical_url: "https://parkinsonspathways.com/agent/trials/NCT02336841.md"
clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT02336841"
ct_last_update_post_date: 2015-01-13
last_seen_at: "2026-05-12T06:20:35.285Z"
source: ClinicalTrials.gov (mirrored, no enrichment)
---
# Self-Help And Recovery Guide in Eating Disorders

**Official Title:** A Study of the Feasibility and Effectiveness of the Addition of Self Help And Recovery Guide for Eating Disorders (SHARED) to Treatment as Usual for Anorexia Nervosa

**NCT ID:** [NCT02336841](https://clinicaltrials.gov/study/NCT02336841)

## Key Facts

- **Status:** UNKNOWN
- **Phase:** EARLY_PHASE1
- **Study Type:** INTERVENTIONAL
- **Target Enrollment:** 150
- **Lead Sponsor:** King's College London
- **Conditions:** Anorexia Nervosa
- **Start Date:** 2015-01
- **Completion Date:** 2017-10
- **CT.gov Last Update:** 2015-01-13

## Brief Summary

The aim of this study is to test a novel guided self-help intervention for patients with Anorexia Nervosa. The 6-week intervention includes the use of self-help materials (i.e. a workbook and short video-clips) and weekly guidance from a peer mentor (i.e. a person recovered from Anorexia Nervosa). Self-reports will be completed at baseline, end of 6 weeks, and 6- and 12 months follow-up. Participants interested in taking part will be randomly allocated to one of two groups.

## Detailed Description

This trial investigates whether a guided self-care intervention (Recovery MANTRA) is a useful addition to treatment as usual (TAU) for individuals with anorexia nervosa (AN). Recovery MANTRA, a 6-week self-care intervention supplemented by peer mentorship, is a module extension of the Maudsley Model of Treatment for Adults with AN and targets the maintenance factors identified by the cognitive-interpersonal model of the illness.

Patients accessing outpatient services for AN are randomised to either TAU or TAU plus Recovery MANTRA. Outcomes variables include changes in body weight at the end of the intervention (primary) and changes in body weight and eating disorder symptoms at immediate and extended follow-ups (6-months and 12-months; secondary). Change is also assessed for the domains identified by the theoretical model, including, motivation, hope, confidence to change, positive mood, cognitive flexibility, therapeutic alliance and social adjustment. Feedback from peer mentors is gathered to understand the impact of providing guidance on their own well-being.

Results from this exploratory investigation will determine whether a larger clinical trial is justifiable and feasible for this affordable intervention which has potential for high reach and scalability.

## Eligibility

- **Minimum age:** 16 Years
- **Sex:** ALL
- **Healthy Volunteers:** No

```
Inclusion Criteria:

\- Referral to one of the participating specialist adult outpatient eating disorder clinics with a primary DSM-5 diagnosis of Anorexia Nervosa or OSFED (Other Specified Feeding or Eating Disorder) with a body mass index (BMI; kg/m2) of 18.5 or below. OSFED will be defined as having features of Anorexia but missing at least two of the four diagnostic criteria.

Exclusion Criteria:

* Insufficient knowledge of English
* Severe mental or physical illness needing treatment in its own right (e.g. psychosis or diabetes mellitus).
```

## Arms

- **Intervention** (EXPERIMENTAL) — Participants in this condition will receive the guided self-help intervention.
- **Control** (ACTIVE_COMPARATOR) — Participants in this condition will not receive the guided self-help intervention. They will receive treatment as usual and weekly feedback on their eating disorder symptoms for a period of 6 weeks.

## Interventions

- **Treatment as usual + Recovery MANTRA** (OTHER) — Participants in this group will receive the guided self-help intervention including video-clips, a workbook, and guidance from peer mentors, and treatment as usual.
- **Treatment as usual + feedback** (OTHER) — Participants in this group will receive treatment as usual and feedback on their eating disorder symptoms.

## Primary Outcomes

- **Changes in body weight at the end of the intervention** _(time frame: 3 years)_

## Secondary Outcomes

- **Changes in eating disorder symptoms at the end of the intervention and follow-up** _(time frame: 3 years)_

## Locations (1)

- King's College London, London, United Kingdom

## Recent Field Changes (last 30 days)

- `eligibility.sex` — added _(2026-05-12)_
- `outcomes.primary` — added _(2026-05-12)_
- `status.overallStatus` — added _(2026-05-12)_
- `status.primaryCompletionDate` — added _(2026-05-12)_
- `status.completionDate` — added _(2026-05-12)_
- `status.lastUpdatePostDate` — added _(2026-05-12)_
- `design.phases` — added _(2026-05-12)_
- `design.enrollmentCount` — added _(2026-05-12)_
- `eligibility.criteria` — added _(2026-05-12)_
- `eligibility.minAge` — added _(2026-05-12)_
- `outcomes.secondary` — added _(2026-05-12)_
- `armsInterventions.arms` — added _(2026-05-12)_
- `armsInterventions.interventions` — added _(2026-05-12)_
- `sponsor.lead` — added _(2026-05-12)_
- `results.hasResults` — added _(2026-05-12)_
- `locations.king's college london|london||united kingdom` — added _(2026-05-12)_

---

*Canonical: https://parkinsonspathways.com/agent/trials/NCT02336841.md*  
*Source data (authoritative): https://clinicaltrials.gov/study/NCT02336841*  
*This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*
