Phone addiction headache? talking therapy may help
NCT ID NCT06631222
First seen Jun 27, 2026 · Last updated Sep 17, 2026 · Updated 2 times
Summary
This study tests whether adding cognitive behavior therapy to physical therapy can reduce tension headaches in adults who are addicted to their smartphones. Forty participants aged 19-34 will receive 12 sessions over 6 weeks. The goal is to see if this combined approach improves headache intensity, neck pain sensitivity, and forward head posture better than physical therapy alone.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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64 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 to 34 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects were those diagnosed with tension type headache by neurologists based on the criteria of the International Headache Society. * age between 19-34. * International Headache Society diagnostic criteria of tension type headaches: * Frequent ETTH or CTTH diagnosed, in both cases more than three months. * Episodes of pain from 30 minutes to 7 days Fulfil 2 or more of the following characteristics: * Bilateral location of pain. * Non-pulsatile pain pressure. * Pain mild to moderate. * The headache does not increase with physical activity. * The headache may be associated with pericranial tenderness. * Controlled pharmacologically. * Myofascial TrPs were bilaterally explored in upper trapezius, splenius capitis, sternocleidomastoid, masseter, superior oblique, levator scapulae and suboccipital muscles, TrP diagnosis was conducted following the diagnostic criteria: * presence of a palpable taut band within a skeletal muscle. * presence of a hypersensitive tender spot in the taut band. * local twitch response elicited by snapping palpation of the taut band reproduction of the typical referred pain pattern of the TrP in response to compression. * TrPs were considered active if both the local and the referred pain evoked by manual palpation reproduced total or partial pattern of the headache. * Patients with FHP who have craniovertebral angle less than 49 degrees were included. Forward head posture is measured by calculating the angle between the horizontal line passing through C7 and a line extending from the tragus of the ear to C7. * patients with smartphone addiction who will score 31 for males and 33 for females on smartphone addiction scale - short version. Exclusion Criteria: * rheumatoid arthritis. * suspected malignancy. * pregnancy. * if they had received manual therapy treatment in the 2 months before enrolment into the study. * Patients with infrequent episodic tension type headache, or with probable frequent and infrequent forms of tension type headache or other concomitant headache. * They can never have vomiting or headache episodes during the treatment. * Episodic tension type headache patients may experience very occasionally photophobia or phonophobia during their episodes of headache. * Chronic tension type headache patients may experience very occasionally photophobia, phonophobia or mild nausea during headache episodes. * Pain aggravated by movement of the head. * Metabolic or musculoskeletal problems with similar headache symptoms. * Previous trauma to the cervical spine. * Active vertigo history. * Poorly controlled hypertension. * Atherosclerosis. * Advanced osteoarthritis. * Patients undergoing pharmacological adaptation or changes in the prophylactic medication. * Excessive emotional stress. * Patients with heart devices. * Joint instability. * Neurological disorders. * Laxity of cervical soft tissues. * Radiographic abnormalities. * Generalized hyperlaxity or hypermobility.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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the British University in Egypt
Cairo, Cairo Governorate, Egypt
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Other studies related to the condition(s) this trial covers.
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