Anorexia NervosaAPAMAdomNCT05803707
Home-based Adapted Physical Activity in Anorexia Nervosa: a Feasibility Pilot Study
A study testing Home-based Adapted Physical Activity in people with Anorexia Nervosa, run by University Hospital, Grenoble at 2 sites in France.
Trial summary
The goal of this pilot clinical trial is to assess a program of Home-based Adapted Physical Activity in Anorexia Nervosa. Read more about this study
- Who is it for?
- Ages 18 to 60 years, women only
- Conditions the study is for
- Anorexia Nervosa
- What is being tested?
- Home-based Adapted Physical Activity
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- 2 sitesFrance
- Study dates
- 22 Sep 2023to 28 Aug 2025
- Phase
- Interventional
- 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 18 to 60 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Female gender
- Age between 18 and 60 years
- Subjects able to give informed consent
- Eating disorders such as anorexia nervosa
- BMI < 18.5 kg/m2
- Affiliated in a social security plan
- Having given informed consent to the research
Who cannot join
- Indication for in-patient care or BMI < 12 kg/m2
- Subject presenting a contrindication to the practice of an adapted physical activity
- Anorexia nervosa in partial or complete remission for more than 1 year
- Patient unable, for technical or any other reason, to connect via the Internet for tele-monitoring and/or tele-rehabilitation
- Persons concerned by the articles L1121-5 to L1121-8 of the public health code
- Subjects who cannot be contacted in case of emergency
- Subjects in a period of exclusion from another study
Trial locations and contacts
2 sites in 1 country.
About this study
The goal of this pilot clinical trial is to assess a program of Home-based Adapted Physical Activity in Anorexia Nervosa.
Read the detailed description
The main questions it aims to answer are: Determining the acceptability of this program / Determining the feasibility and safety of this program / Determining patient satisfaction / Measuring the evolution of the symptomatology. Participants will follow a program of Home-based Adapted Physical Activity.
- Conditions
- Anorexia Nervosa
- Being tested
- Home-based Adapted Physical Activity
- Keywords
- Anorexia Nervosa, telerehabilitation, Adapted Physical Activity
- Medical subject headings
- Anorexia Nervosa
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Home-based Adapted Physical ActivityBehavioural
There will be 8 weekly sessions at a time defined in advance for the same group and for the 8 sessions
| Study group | Role | What they receive |
|---|---|---|
| Home-based Adapted Physical Activity | Experimental | Home-based Adapted Physical Activity sessions by videoconference Receives: Behavioral: Home-based Adapted Physical Activity |
What is being measured
The primary outcome is the main question the study is designed to answer.
Acceptability of a telerehabilitation adapted physical activity (APA) program for patient with anorexia nervosa quantitatively
Number of patients who have realized the first of the 8 adapted physical activity session in relation to the total number of eligibly patients who have been invited to participate at the study
Measured: at the first session of the APA program (Day 0)
Acceptability of a telerehabilitation adapted physical activity program for patient with anorexia nervosa qualitively
Reasons for refusal and participation's age will be collected anonymously for patients who refuse inclusion but agree to this informations being collected
Measured: at the first session of the APA program (Day 0)
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Number and portion of patients who have realized the 8 adapted physical activity sessions as well as the first and final sessions
Measured: at the end-of-study visit (Day 0 + 11 weeks)
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
Motifs of no realization of one ou more sessions will be collected. They will inclued technical problems, personal, professional ou medical constraints inclued study's exit for weight loss
Measured: at the end-of-study visit (Day 0 + 11 weeks)
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Portion of patients answing "yes" at the question : "Would you like to continue this program ?"
Measured: at the final session of APA programm (Day 0 + 8 weeks)
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
Programm's motifs of satisfaction or no satisfaction will be collected during the final session of adapted physical activity program
Measured: at the final session of APA programm (Day 0 + 8 weeks)
Measuring changes in symptomatology in key areas such as self-esteem through self-assessment questionnaire
Determination of this parameter :self-esteem by self-esteem scale of Rosenberg
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as quality of life through self-assessment questionnaire
Determination of this parametes :quality of life by QUAVIAM scale
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as dependence on physical activity through self-assessment questionnaire
Determination of this parameter : dependence on physical activity by EDQ questionnary
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as dependence on physical activity through objective measure
Determination of this parameter : level of physical activity by 7-day actimetry recording
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as changes in weight through objective measure
Determination of this parameter : weight in kilograms on a classic scale
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Measuring changes in symptomatology in key areas such as body composition through objective measure
Determination of this parameters : the body composition will be determinated by a impedancemetry measurement
Measured: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Apr 2023
- Study start22 Sep 2023
- Primary completion28 Aug 2025
- Study completion28 Aug 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Anorexia NervosaStudies of the same condition, open and under way.
- More trials run by University Hospital, GrenobleThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 36 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital, Grenoble
- Sponsor type
- University, hospital or other
- Collaborators
- AGIR à Dom
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05803707
- Sponsor's protocol ID
- 38RC22.0097
- Acronym
- APAMAdom
- Status last verified
- Oct 2025
- First submitted
- 23 Dec 2022
- Last updated
- 7 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Home-based Adapted Physical Activity in Anorexia Nervosa: a Feasibility Pilot Study
- ClinicalTrials.gov ID
- NCT05803707
- Acronym / sponsor ID
- APAMAdom / 38RC22.0097
- Conditions
- Anorexia Nervosa
- Keywords
- Anorexia Nervosa, telerehabilitation, Adapted Physical Activity
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 36 participants (actual)
- Lead sponsor
- University Hospital, GrenobleUniversity, hospital or other
- Collaborators
- AGIR à Dom
- Study start
- 22 Sep 2023 (actual)
- Primary completion
- 28 Aug 2025 (actual)
- Study completion
- 28 Aug 2025 (actual)
- First posted
- 7 Apr 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this pilot clinical trial is to assess a program of Home-based Adapted Physical Activity in Anorexia Nervosa.
Detailed description
The main questions it aims to answer are: Determining the acceptability of this program / Determining the feasibility and safety of this program / Determining patient satisfaction / Measuring the evolution of the symptomatology. Participants will follow a program of Home-based Adapted Physical Activity.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Home-based Adapted Physical Activity | Experimental | Behavioral: Home-based Adapted Physical ActivityHome-based Adapted Physical Activity sessions by videoconference |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (7 listed)
- Female gender
- Age between 18 and 60 years
- Subjects able to give informed consent
- Eating disorders such as anorexia nervosa
- BMI < 18.5 kg/m2
Key exclusion criteria (7 listed)
- Indication for in-patient care or BMI < 12 kg/m2
- Subject presenting a contrindication to the practice of an adapted physical activity
- Anorexia nervosa in partial or complete remission for more than 1 year
- Patient unable, for technical or any other reason, to connect via the Internet for tele-monitoring and/or tele-rehabilitation
- Persons concerned by the articles L1121-5 to L1121-8 of the public health code
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Home-based Adapted Physical ActivityThere will be 8 weekly sessions at a time defined in advance for the same group and for the 8 sessions | Behavioural | Home-based Adapted Physical Activity |
Primary outcome
Acceptability of a telerehabilitation adapted physical activity (APA) program for patient with anorexia nervosa quantitatively
Time frame: at the first session of the APA program (Day 0)
Number of patients who have realized the first of the 8 adapted physical activity session in relation to the total number of eligibly patients who have been invited to participate at the study
Acceptability of a telerehabilitation adapted physical activity program for patient with anorexia nervosa qualitively
Time frame: at the first session of the APA program (Day 0)
Reasons for refusal and participation's age will be collected anonymously for patients who refuse inclusion but agree to this informations being collected
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Time frame: at the end-of-study visit (Day 0 + 11 weeks)
Number and portion of patients who have realized the 8 adapted physical activity sessions as well as the first and final sessions
Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
Time frame: at the end-of-study visit (Day 0 + 11 weeks)
Motifs of no realization of one ou more sessions will be collected. They will inclued technical problems, personal, professional ou medical constraints inclued study's exit for weight loss
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively
Time frame: at the final session of APA programm (Day 0 + 8 weeks)
Portion of patients answing "yes" at the question : "Would you like to continue this program ?"
Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively
Time frame: at the final session of APA programm (Day 0 + 8 weeks)
Programm's motifs of satisfaction or no satisfaction will be collected during the final session of adapted physical activity program
Measuring changes in symptomatology in key areas such as self-esteem through self-assessment questionnaire
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parameter :self-esteem by self-esteem scale of Rosenberg
Measuring changes in symptomatology in key areas such as quality of life through self-assessment questionnaire
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parametes :quality of life by QUAVIAM scale
Measuring changes in symptomatology in key areas such as dependence on physical activity through self-assessment questionnaire
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parameter : dependence on physical activity by EDQ questionnary
Measuring changes in symptomatology in key areas such as dependence on physical activity through objective measure
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parameter : level of physical activity by 7-day actimetry recording
Measuring changes in symptomatology in key areas such as changes in weight through objective measure
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parameter : weight in kilograms on a classic scale
Measuring changes in symptomatology in key areas such as body composition through objective measure
Time frame: at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks )
Determination of this parameters : the body composition will be determinated by a impedancemetry measurement
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 May 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Home-based Adapted Physical Activity in people with Anorexia Nervosa, run by University Hospital, Grenoble at 2 sites in France.
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 7 inclusion and 7 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 7 May 2026. 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 France. 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?
Acceptability of a telerehabilitation adapted physical activity (APA) program for patient with anorexia nervosa quantitatively (time frame: at the first session of the APA program (Day 0)). The study lists 12 primary outcomes in all. 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 7 May 2026.