Chronic Mental DisordersRhMoGYANCT06910488
The Effect of Daily Living Activities Mobile Application Developed for Individuals With Chronic Mental Disorder on Functionality
A study testing Daily Living Activities Mobile Application, Individual interviews and Group education in people with Chronic Mental Disorders, run by Ege University at 1 site in Turkey (Türkiye).
Trial summary
The study was conducted to evaluate the functionality of a mobile application programme developed to help individuals with chronic mental disorders plan and implement their daily activities and its impact on activities of daily living. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Chronic Mental Disorders
- What is being tested?
- Daily Living Activities Mobile Application, Individual interviews and Group education
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 57 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Apr 2024to 18 Oct 2024
- 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 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
None listed.
Who cannot join
- Hearing, vision, speech and comprehension problems
- Individuals who did not attend the two scheduled sessions
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Ege University Faculty of Medicine Hospital/ Department of Mental Health and Diseases
Izmir
About this study
Official title: Daily Living Activities Mobile Application Program
The study was conducted to evaluate the functionality of a mobile application programme developed to help individuals with chronic mental disorders plan and implement their daily activities and its impact on activities of daily living.
The main questions it aims to answer are:
Does the activities of daily living mobile application programme improve participants' activities of daily living? Does the activities of daily living mobile application programme improve the activities of daily living? Does the activities of daily living mobile application programme improve participants' medication adherence?
Read the detailed description
This study was conducted to evaluate the effect of a mobile application program developed to enable individuals with chronic mental disorders to plan and implement their daily activities on their functionality, daily activities, and medication adherence.
The study was designed as an experimental study with a control group, including pre-test, post-test, and follow-up measurements. A total of 64 patients with chronic mental disorders who met the inclusion criteria were included in the study, with 32 in the intervention group and 32 in the control group. Data were collected using the Introductory Information Form, the Social Functioning Assessment Scale (SFAS), the Lawton Instrumental Activities of Daily Living (IADL) Scale, and the Morisky Medication Adherence Scale (MMAS). Participants in the intervention group were administered the Activities of Daily Living-Based Mobile Application Programme developed in this study.
- Conditions
- Chronic Mental Disorders
- Being tested
- Daily Living Activities Mobile Application, Individual interviews, Group education, Routine rehabilitation program
- Keywords
- chronic mental disorders, mobile application, activities of daily living model, functionality, psychiatric nursing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Daily Living Activities Mobile ApplicationOther
Also called Experimental group
mobile application was used for three months
Individual interviewsOther
The individual's daily living activities are assessed using forms and scales that evaluate disability, functional level, and the ability to perform skill-based activities.
Factors affecting daily living activities, such as strengths and weaknesses, barriers, accessible healthcare services, and social support networks, are examined.
The client's independent, semi-dependent, and dependent daily living activities are evaluated together.
Implementation steps are created to achieve the identified goals. Barriers to achieving the goals and supporting factors are identified.
Group educationOther
Information is provided about the symptoms of schizophrenia and bipolar disorder, their causes, and treatment.
The early warning signs are explained, along with the importance of recognizing that they can lead to an emergency situation.
The importance of prior planning for what to do in case of an emergency is discussed. As homework, the family is asked to make this plan together.
Information is provided about the importance of daily living activities and what they entail.
Information is provided about self-care skills, healthy nutrition, movement planning, good sleep hygiene, the importance of body temperature regulation, and elimination issues.
Information is provided about communication skills. Information is given about what to pay attention to in order to establish effective communication.
Routine rehabilitation programOther
It includes psychiatric rehabilitation services that are part of the clinic's program.
| Study group | Role | What they receive |
|---|---|---|
| Experimental group | Active comparator | In the study, an individual-specific rehabilitation programme consisting of diagnosis, planning and intervention stages was created for the patients included in the intervention group.
In addition to routine rehabilitation services, the activities of daily living mobile application programme was applied to the intervention group in the form of face-to-face individual interviews, group training, use of RhMoGYA application by the patients for three months, and planning and follow-up of activities for the use of patients by the researcher.
The interviews were planned within the scope of the Roper Activities of Daily Living Model for the development and follow-up of patients' activities of daily living. Receives: Other: Daily Living Activities Mobile Application; Other: Individual interviews; Other: Group education; Other: Routine rehabilitation program |
| Control group | Experimental | A routine rehabilitation program has been followed Receives: Other: Routine rehabilitation program |
What is being measured
The primary outcome is the main question the study is designed to answer.
Social Functioning Assessment Scale
The evaluation range of the scale is 19 to 57 points. High score is interpreted as high level of functionality.
Measured: Baseline and 5 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2025
- Study start1 Apr 2024
- Primary completion15 Apr 2024
- Study completion18 Oct 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Mental DisordersStudies of the same condition, open and under way.
- More trials run by Ege UniversityThe 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- In addition to routine rehabilitation services, activities of daily living mobile application programme was applied to the intervention group. The control group received routine rehabilitation services.
- Masking
- None (open label)
- Enrolment
- 57 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ege University
- Sponsor type
- University, hospital or other
- Collaborators
- The Scientific and Technological Research Council of Turkey
- Responsible party
- Principal investigator, SENEM ONOL, Ege University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06910488
- Sponsor's protocol ID
- Decision No: 22-2.1T/27
- Acronym
- RhMoGYA
- Status last verified
- Mar 2025
- First submitted
- 19 Mar 2025
- Last updated
- 4 Apr 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All collected IPD
Study at a glance
From the registry record, last updated by the sponsor on 4 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Daily Living Activities Mobile Application Program
- ClinicalTrials.gov ID
- NCT06910488
- Acronym / sponsor ID
- RhMoGYA / Decision No: 22-2.1T/27
- Conditions
- Chronic Mental Disorders
- Keywords
- chronic mental disorders, mobile application, activities of daily living model, functionality, psychiatric nursing
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 57 participants (actual)
- Lead sponsor
- Ege UniversityUniversity, hospital or other
- Collaborators
- The Scientific and Technological Research Council of Turkey
- Study start
- 1 Apr 2024 (actual)
- Primary completion
- 15 Apr 2024 (actual)
- Study completion
- 18 Oct 2024 (actual)
- First posted
- 4 Apr 2025 (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 study was conducted to evaluate the functionality of a mobile application programme developed to help individuals with chronic mental disorders plan and implement their daily activities and its impact on activities of daily living.
The main questions it aims to answer are:
Does the activities of daily living mobile application programme improve participants' activities of daily living? Does the activities of daily living mobile application programme improve the activities of daily living? Does the activities of daily living mobile application programme improve participants' medication adherence?
Detailed description
This study was conducted to evaluate the effect of a mobile application program developed to enable individuals with chronic mental disorders to plan and implement their daily activities on their functionality, daily activities, and medication adherence.
The study was designed as an experimental study with a control group, including pre-test, post-test, and follow-up measurements. A total of 64 patients with chronic mental disorders who met the inclusion criteria were included in the study, with 32 in the intervention group and 32 in the control group. Data were collected using the Introductory Information Form, the Social Functioning Assessment Scale (SFAS), the Lawton Instrumental Activities of Daily Living (IADL) Scale, and the Morisky Medication Adherence Scale (MMAS). Participants in the intervention group were administered the Activities of Daily Living-Based Mobile Application Programme developed in this study.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- In addition to routine rehabilitation services, activities of daily living mobile application programme was applied to the intervention group. The control group received routine rehabilitation services.
| Arm | Type | Receives |
|---|---|---|
| Experimental group | Active comparator | Other: Daily Living Activities Mobile Application, Other: Individual interviews, Other: Group education, Other: Routine rehabilitation programIn the study, an individual-specific rehabilitation programme consisting of diagnosis, planning and intervention stages was created for the patients included in the intervention group. In addition to routine rehabilitation services, the activities of daily living mobile application programme was applied to the intervention group in the form of face-to-face individual interviews, group training, use of RhMoGYA application by the patients for three months, and planning and follow-up of activities for the use of patients by the researcher. The interviews were planned within the scope of the Roper Activities of Daily Living Model for the development and follow-up of patients' activities of daily living. |
| Control group | Experimental | Other: Routine rehabilitation programA routine rehabilitation program has been followed |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (0 listed)
Key exclusion criteria (2 listed)
- Hearing, vision, speech and comprehension problems
- Individuals who did not attend the two scheduled sessions
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 |
|---|---|---|
| Daily Living Activities Mobile ApplicationAlso: Experimental groupmobile application was used for three months | Other | Experimental group |
| Individual interviewsThe individual's daily living activities are assessed using forms and scales that evaluate disability, functional level, and the ability to perform skill-based activities. Factors affecting daily living activities, such as strengths and weaknesses, barriers, accessible healthcare services, and social support networks, are examined. The client's independent, semi-dependent, and dependent daily living activities are evaluated together. Implementation steps are created to achieve the identified goals. Barriers to achieving the goals and supporting factors are identified. | Other | Experimental group |
| Group educationInformation is provided about the symptoms of schizophrenia and bipolar disorder, their causes, and treatment. The early warning signs are explained, along with the importance of recognizing that they can lead to an emergency situation. The importance of prior planning for what to do in case of an emergency is discussed. As homework, the family is asked to make this plan together. Information is provided about the importance of daily living activities and what they entail. Information is provided about self-care skills, healthy nutrition, movement planning, good sleep hygiene, the importance of body temperature regulation, and elimination issues. Information is provided about communication skills. Information is given about what to pay attention to in order to establish effective communication. | Other | Experimental group |
| Routine rehabilitation programIt includes psychiatric rehabilitation services that are part of the clinic's program. | Other | Control group, Experimental group |
Primary outcome
Social Functioning Assessment Scale
Time frame: Baseline and 5 months
The evaluation range of the scale is 19 to 57 points. High score is interpreted as high level of functionality.
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 4 Apr 2025.
- Individual participant dataSharing planned: Yes. All collected IPD
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Daily Living Activities Mobile Application, Individual interviews and Group education in people with Chronic Mental Disorders, run by Ege University at 1 site in Turkey (Türkiye).
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 0 inclusion and 2 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 4 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). 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?
Social Functioning Assessment Scale (time frame: Baseline and 5 months). 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 4 Apr 2025.